-
Mashup Score: 0Thread by @jamil_tajik on Thread Reader App - 1 year(s) ago
@AJamilTajik: Fabry’s CM is an X-linked inherited deficiency of alpha-galactosidase A which results in systemic sphingolipid accumulation. Severity of manifestation depends on degree of X-chromosome inactivation => ……
Source: threadreaderapp.comCategories: Cardiologists, Latest HeadlinesTweet
#Fabrys Thread by @jamil_tajik on Thread Reader App I still learn from him 25 years after finishing my #CVFellowship ! https://t.co/wt4nIxhVb3