Homozygous MYH7 R1820W mutation results in recessive myosin storage myopathy: scapuloperoneal and respiratory weakness with dilated cardiomyopathy. (Q51660072)
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scientific article published on 26 January 2015
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Homozygous MYH7 R1820W mutation results in recessive myosin storage myopathy: scapuloperoneal and respiratory weakness with dilated cardiomyopathy. |
scientific article published on 26 January 2015 |
Statements
Homozygous MYH7 R1820W mutation results in recessive myosin storage myopathy: scapuloperoneal and respiratory weakness with dilated cardiomyopathy (English)
Özgecan Ayhan
26 January 2015