Konu "obscurin" için Fakülteler / Faculties listeleme
Toplam kayıt 1, listelenen: 1-1
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Bi-Allelic Loss-Of-Function OBSCN Variants Predispose Individuals to Severe Recurrent Rhabdomyolysis
(2021)Rhabdomyolysis is the acute breakdown of skeletal myofibres in response to an initiating factor, most commonly toxins and over exertion. A variety of genetic disorders predispose to rhabdomyolysis through different pathogenic ...