Patients with Familial Partial Lipodystrophy of the Dunnigan Type Due to aLMNAR482W Mutation Show Muscular and Cardiac Abnormalities-Reference-Cited by-同舟云学术

Patients with Familial Partial Lipodystrophy of the Dunnigan Type Due to aLMNAR482W Mutation Show Muscular and Cardiac Abnormalities

Published:2004-11 Issue:11 Volume:89 Page:5337-5346
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:The Journal of Clinical Endocrinology & Metabolism

Author:

Vantyghem M. C.,Pigny P.,Maurage C. A.,Rouaix-Emery N.,Stojkovic T.,Cuisset J. M.,Millaire A.,Lascols O.,Vermersch P.,Wemeau J. L.,Capeau J.,Vigouroux C.

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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