DOI:
10.1055/s-00000041
Neuropediatrics
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References
Brockington M, Blake DJ, Prandini P. , et al.
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.
Am J Hum Genet 2001;
69 (06) 1198-1209
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