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CGI-58, the Causative Gene for Chanarin-Dorfman Syndrome, Mediates Acylation of Lysophosphatidic Acid

cgi-58 (comparative gene identification-58) is a member of α/β-hydrolase family of proteins. Mutations in CGI-58 are shown to be responsible for a rare genetic disorder known as Chanarin-Dorfman syndrome, characterized by an excessive accumulation of triacylglycerol in several tissues and ichthyosis...

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Detalhes bibliográficos
Main Authors: Ghosh, Ananda K., Ramakrishnan, Geetha, Chandramohan, Chitraju, Rajasekharan, Ram
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Biochemistry and Molecular Biology 2008
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3259832/
https://ncbi.nlm.nih.gov/pubmed/18606822
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M801783200
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