Cerebral lipid accumulation in Chanarin–Dorfman Syndrome-Reference-Cited by-同舟云学术

Cerebral lipid accumulation in Chanarin–Dorfman Syndrome

Published:2015-01 Issue:1 Volume:114 Page:51-54
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Huigen Marleen C.D.G.,van der Graaf Marinette,Morava Eva,Dassel A. Carin M.,van Steensel Maurice A.M.,Seyger Marieke M.B.,Wevers Ron A.,Willemsen Michèl A.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference29 articles.

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3. Chanarin–Dorfman syndrome: deficiency in CGI-58, a lipid droplet-bound co-activator of lipase;Yamaguchi;Biochim. Biophys. Acta,2009

4. Dorfman–Chanarin syndrome (neutral lipid storage disease): new clinical features;Peña-Penabad;Br. J. Dermatol.,2001

5. Spatial localization in NMR spectroscopy in vivo;Bottomley;Ann. N. Y. Acad. Sci.,1987

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