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Mutations at the lysosomal acid cholesteryl ester hydrolase gene locus in Wolman disease.

The genomic sequences encoding the human lysosomal acid lipase/cholesteryl esterase (sterol esterase; EC 3.1.1.13) have been isolated and sequenced, and the information has been used to identify mutations in both alleles of the gene from a patient with Wolman disease, an autosomal recessive lysosoma...

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Autors principals: Anderson, R A, Byrum, R S, Coates, P M, Sando, G N
Format: Artigo
Idioma:Inglês
Publicat: 1994
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC43441/
https://ncbi.nlm.nih.gov/pubmed/8146180
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