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Congenital Myopathy 9B
A congenital myopathy that is neonatal hypotonia followed by mildly delayed walking in childhood, mainly affecting proximal muscles, and that is caused by homozygous mutation in the FXR1 gene on chromosome 3q28. Bialleli
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Overview
A congenital myopathy that is neonatal hypotonia followed by mildly delayed walking in childhood, mainly affecting proximal muscles, and that is caused by homozygous mutation in the FXR1 gene on chromosome 3q28. Bialleli
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