Nemaline Myopathy 6 (NEM6)

Alias:

Nemaline Myopathy 6, Autosomal Dominant

Nem6

Myopathy, Nemaline, Type 6

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Nemaline Myopathy 6, also known as nem6, is related to nemaline myopathy and myopathy, and has symptoms including muscular stiffness An important gene associated with Nemaline Myopathy 6 is KBTBD13 (Kelch Repeat And BTB Domain Containing 13). Affiliated tissues include skeletal muscle, and related phenotypes are gait disturbance and facial palsy

Related ID：

MALACARDS：NML007

OMIM：609273

MESH：C538398