nemaline myopathy 4 (Q32144895)
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nemaline myopathy that has material basis in heterozygous mutation in the TPM2 gene on chromosome 9p13
- nemaline myopathy 4, autosomal dominant
- NEM4
- NEMALINE MYOPATHY 4; NEM4
- Cap Myopathy 2
- Nemaline Myopathy type 4
- NEMALINE MYOPATHY 4
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | nemaline myopathy 4 |
nemaline myopathy that has material basis in heterozygous mutation in the TPM2 gene on chromosome 9p13 |
|
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C164225
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