nemaline myopathy 11 (Q32144908)
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nemaline myopathy characterized by onset of slowly progressive muscle weakness in the first decade of life that has material basis in homozygous or compound heterozygous mutation in the MYPN gene on chromosome 10q21
- NEM11
- nemaline myopathy 11, autosomal recessive
- nemaline myopathy type 11
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | nemaline myopathy 11 |
nemaline myopathy characterized by onset of slowly progressive muscle weakness in the first decade of life that has material basis in homozygous or compound heterozygous mutation in the MYPN gene on chromosome 10q21 |
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Statements
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Identifiers
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