DOI: 10.1055/s-00000071

Seminars in Neurology

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 (6) 1198-1209

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