| 1 | CHAC, MCLDP, XK, FHBL1,FHBL2,ABL, APOB
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| Neuroacanthocytosis.
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| Danek A, Walker RH.
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| Curr Opin Neurol 18(4):386-92. Review. 2005
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| 2 | TRPM7, XK, MCLDP
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| Neuroacanthocytosis: new developments in a neglected group of dementing disorders.
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| Danek A, Jung HH, Melone MA, Rampoldi L, Broccoli V, Walker RH.
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| J Neurol Sci 229-230:171-86. Epub 2005 Jan 7. Review. 2005
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| 3 | XK, MCLDP
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| McLeod syndrome: a novel mutation, predominant psychiatric manifestations, and distinct striatal imaging findings.
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| Jung HH, Hergersberg M, Kneifel S, Alkadhi H, Schiess R, Weigell-Weber M, Daniels G, Kollias S, Hess K.
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| Ann Neurol 49(3):384-92. 2001
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| 4 | XK, MCLDP
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| McLeod neuroacanthocytosis: genotype and phenotype.
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| Danek A, Rubio JP, Rampoldi L, Ho M, Dobson-Stone C, Tison F, Symmans WA, Oechsner M, Kalckreuth W, Watt JM, Corbett AJ, Hamdalla HH, Marshall AG, Sutton I, Dotti MT, Malandrini A, Walker RH, Daniels G, Monaco AP.
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| Ann Neurol 50(6):755-64. 2001
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| 5 | MCLDP
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| A novel mutation of the McLeod syndrome gene in a Japanese family.
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| Ueyama H, Kumamoto T, Nagao S, Masuda T, Sugihara R, Fujimoto S, Tsuda T.
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| J Neurol Sci 176(2):151-4. 2000
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| 6 | MCLDP
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| Analysis of the McLeod syndrome gene in three patients with neuroacanthocytosis.
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| Shizuka M, Watanabe M, Aoki M, Ikeda Y, Mizushima K, Okamoto K, Itoyama Y, Abe K, Shoji M.
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| J Neurol Sci 150(2):133-5. 1997
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| 7 | MCLDP, XK
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| Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein.
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| Ho M, et al.
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| Cell 77 : 869-880. 1994
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| 8 | DXS709, MCLDP
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| Fine mapping of the McLeod locus (XK) to a 150-380-kb region in Xp21.
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| Ho MF, et al.
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| Am J Hum Genet 50 : 317-330. 1992
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| 9 | MCLDP, CYBB, RP3, OTC
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| Physical mapping of the McLeod locus and isolation of a 1.7Mb contig containing genes for McLeod, chronic granulomatous disease (CGD), retinitis pigmentosa form 3, (RP3) and ornithine transcarbamylase (OTC).
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| Ho M, et al.
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| (HGM11) Cytogenet Cell Genet 58 : 2067. 1991
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| 10 | MCLDP
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| Dystrophin expression and genotypic analysis of two cases of benign X linked myopathy (McLeod's syndrome).
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| Carter ND, et al.
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| J Med Genet 27 : 345-347. 1990
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| 11 | MCLDP
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| Gene deletion in a patient with chronic granulomatous disease and McLeod syndrome: fine mapping of the Xk gene locus.
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| Frey D, et al.
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| Blood 71 : 252-255. 1988
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| 12 | MCLDP, XK
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| Localization of the McLeod locus (XK) within Xp21 by deletion analysis.
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| Bertelson CJ, et al.
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| Am J Hum Genet 42 : 703-711. 1988
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| 13 | CYBB, MCLDP, RP3, DXS307
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| Xp21 DNA microdeletion in a patient with chronic granulomatous disease, retinitis pigmentosa, and McLeod phenotype.
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| Saint Basile G de, et al.
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| Hum Genet 80 : 85-89. 1988
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| 14 | MCLDP, CYBB, DMD, DXS28
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| Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome.
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| Francke U, Ochs HD, de Martinville B, Giacalone J, Lindgren V, Disteche C, Pagon RA, Hofker MH, van Ommen GJ, Pearson PL, et al.
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| Am J Hum Genet 37 : 250-267. 1985
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