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pro vyhledávání: '"Fatiha Benmiloud"'
Publikováno v:
Apollo Medicine, Vol 17, Iss 4, Pp 272-274 (2020)
Cholesteryl ester storage disease (CESD) in children is a rare anatomo-clinical entity, characterized by a secondary lysosomal accumulation and an autosomal recessive mutation in the LIPA gene, which results from a lysosomal acid lipase (LAL) deficie
Externí odkaz:
https://doaj.org/article/755ef849e93941f0b86febcced17c6dc
Publikováno v:
Apollo Medicine, Vol 17, Iss 4, Pp 272-274 (2020)
Cholesteryl ester storage disease (CESD) in children is a rare anatomo-clinical entity, characterized by a secondary lysosomal accumulation and an autosomal recessive mutation in the LIPA gene, which results from a lysosomal acid lipase (LAL) deficie