Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin a2 deficiency and abnormal glycosylation of a-dystroglycan

• BROCKINGTON M

収録刊行物

• American Journal of Human Genetics

  American Journal of Human Genetics 69 1198-1209, 2001

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• CRID: 1573950400349971712
• NII論文ID: 10021226197
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