← Назад
🧬

MYL1

myosin light chain 1

gene with protein productOMIM: 1607801 заболевание
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Disease-causing germline mutation(s) (loss of function) in1
Congenital myopathy with reduced type 2 muscle fibersORPHA:544602
→
Данные: Orphadata (CC-BY-4.0)