| 1 | MEAX, VMA21
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| X-linked myopathy: when autophagy goes wrong.
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| Mazarei G.
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| Clin Genet 77(2):114-5. Epub 2009 Nov 11. No abstract available. PMID: 19912261 2010
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| 2 | LAMP2,MEAX
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| A new congenital form of X-linked autophagic vacuolar myopathy.
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| Yan C, Tanaka M, Sugie K, Nobutoki T, Woo M, Murase N, Higuchi Y, Noguchi S, Nonaka I, Hayashi YK, Nishino I.
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| Neurology 65(7):1132-4. 2005
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| 3 | LAMP2, MEAX
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| Expression of the lysosome-associated membrane proteins in myopathies with rimmed vacuoles.
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| Tsuruta Y, Furuta A, Furuta K, Yamada T, Kira J, Iwaki T.
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| Acta Neuropathol (Berl) 101(6):579-84. 2001
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| 4 | MEAX
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| Linkage of X-linked myopathy with excessive autophagy (XMEA) to Xq28.
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| Villard L, des Portes V, Levy N, Louboutin JP, Recan D, Coquet M, Chabrol B, Figarella-Branger D, Chelly J, Pellissier JF, Fontes M.
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| Eur J Hum Genet 8(2):125-9. 2000
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| 5 | MEAX
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| X-linked vacuolar myopathies: two separate loci and refined genetic mapping.
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| Auranen M, Villanova M, Muntoni F, Fardeau M, Scherer SW, Kalino H, Minassian BA.
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| Ann Neurol 47(5):666-9. 2000
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| 6 | APOA1, LAMP2, MEAX, NNHA
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| The new apolipoprotein A-I variant leu(174) --> Ser causes hereditary cardiac amyloidosis, and the amyloid fibrils are constituted by the 93-residue N-terminal polypeptide.
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| Obici L, Bellotti V, Mangione P, Stoppini M, Arbustini E, Verga L, Zorzoli I, Anesi E, Zanotti G, Campana C, Vigaṇ M, Merlini G.
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| Am J Pathol 155(3):695-702. 1999
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| 7 | MEAX
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| Linkage analysis for X-linked myopathy with excessive autophagy.
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| Carpenter NJ, et al.
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| Am J Hum Genet 49S : 337. 1991
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| 8 | MEAX
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| Linkage studies in a new X-linked myopathy, suggesting exclusion of DMD locus and tentative assignment to distal Xq.
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| Saviranta P, et al.
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| Am J Hum Genet 42 : 84-88. 1988
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