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pro vyhledávání: '"Mira Almheiri"'
Autor:
Manal Mustafa, Mira Almheiri
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 29, Iss 2, Pp 130-134 (2024)
Familial chylomicronemia syndrome (FCS) is a rare autosomal recessive disease affecting lipoprotein metabolism. FCS is estimated to occur in 1 in 1–2 million individuals and can be diagnosed at any age, equally affecting all genders, races, and eth
Externí odkaz:
https://doaj.org/article/637a5610c1c64ae28dc5c44fe6af0225