centronuclear myopathy 4 (Q66084920)
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An autosomal dominant centronuclear myopathy that has material basis in heterozygous mutation in CCDC78 on 16p13.3.
- CNM4
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | centronuclear myopathy 4 |
An autosomal dominant centronuclear myopathy that has material basis in heterozygous mutation in CCDC78 on 16p13.3. |
|
Statements
1 reference
Identifiers
1 reference
1 reference