| congenitale myopathie met vezeltypedisproportie door mutatie van 'myosin heavy chain 7' (aandoening) |
| congenitale myopathie met vezeltypedisproportie door mutatie van 'myosin heavy chain 7' |
| congenitale 'fiber-type disproportion myopathy' door mutatie van MYH7
CFTDM door MYH7-mutatie
|
| Congenital fiber-type disproportion myopathy due to MYH7 mutation |
| Congenital fiber-type disproportion myopathy due to myosin heavy chain 7 mutation
|
| Congenital myopathy with fiber-type disproportion associated with the MYH7 (myosin heavy chain 7) gene on the cytogenetic location 14q11.2 inherited in an autosomal dominant manner. |
