Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan (Q24535942)
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(P577) Monday, October 8, 2001
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(P1476) "Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan" (language: en)
(P2093) M Brockington
D J Blake
P Prandini
S Torelli
M A Benson
B Estournet
N B Romero
E Mercuri
T Voit
C A Sewry
F Muntoni
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