(Q32144919)
English
nemaline myopathy 7
nemaline myopathy characterized by very early onset of hypotonia and delayed motor development that has material basis in homozygous mutation in the CFL2 gene on chromosome 14q13
- NEM7
- nemaline myopathy 7, autosomal recessive
- Nemaline Myopathy type 7
- NEMALINE MYOPATHY 7; NEM7
- NEMALINE MYOPATHY 7
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