Citations for
1CHAC, MCLDP, XK, FHBL1,FHBL2,ABL, APOB
Neuroacanthocytosis.
Danek A, Walker RH.
Curr Opin Neurol 18(4):386-92. Review. 2005
2TRPM7, XK, MCLDP
Neuroacanthocytosis: new developments in a neglected group of dementing disorders.
Danek A, Jung HH, Melone MA, Rampoldi L, Broccoli V, Walker RH.
J Neurol Sci 229-230:171-86. Epub 2005 Jan 7. Review. 2005
3XK
McLeod phenotype associated with a XK missense mutation without hematologic, neuromuscular, or cerebral involvement.
Jung HH, Hergersberg M, Vogt M, Pahnke J, Treyer V, Rothlisberger B, Kollias SS, Russo D, Frey BM.
Transfusion 43(7):928-38. 2003
4XK, MCLDP
McLeod syndrome: a novel mutation, predominant psychiatric manifestations, and distinct striatal imaging findings.
Jung HH, Hergersberg M, Kneifel S, Alkadhi H, Schiess R, Weigell-Weber M, Daniels G, Kollias S, Hess K.
Ann Neurol 49(3):384-92. 2001
5XK, MCLDP
McLeod neuroacanthocytosis: genotype and phenotype.
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.
Ann Neurol 50(6):755-64. 2001
6XK
Intracellular assembly of Kell and XK blood group proteins.
Russo D, Lee S, Redman C.
Biochim Biophys Acta 1461(1):10-8. 1999
7XK
Kell and Kx, two disulfide-linked proteins of the human erythrocyte membrane are phosphorylated in vivo.
Carbonnet F, Hattab C, Cartron JP, Bertrand O.
Biochem Biophys Res Commun 247(3):569-75. 1998
8XK
Kx, a quantitatively minor protein from human erythrocytes, is palmitoylated in vivo.
Carbonnet F, Hattab C, Callebaut I, Cochet S, Blancher A, Cartron JP, Bertrand O.
Biochem Biophys Res Commun 250(3):569-74. 1998
9XK
Immunochemical analysis of the Kx protein from human red cells of different Kell phenotypes using antibodies raised against synthetic peptides.
Carbonnet F, Hattab C, Collec E, Le van Kim C, Cartron JP, Bertrand O.
Br J Haematol 96(4):857-63. 1997
10MCLDP, XK
Localization of the McLeod locus (XK) within Xp21 by deletion analysis.
Bertelson CJ, et al.
Am J Hum Genet 42 : 703-711. 1988