Mutations inGng3lgandAGPAT2in Berardinelli-Seip Congenital Lipodystrophy and Brunzell Syndrome: Phenotype Variability Suggests Important Modifier Effects-Reference-Cited by-同舟云学术

Mutations inGng3lgandAGPAT2in Berardinelli-Seip Congenital Lipodystrophy and Brunzell Syndrome: Phenotype Variability Suggests Important Modifier Effects

Published:2004-06 Issue:6 Volume:89 Page:2916-2922
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:The Journal of Clinical Endocrinology & Metabolism

Author:

Fu Mao,Kazlauskaite Rasa,Paiva Baracho Maria de Fátima,Nascimento Santos Maria Goretti Do,Brandão-Neto José,Villares Sandra,Celi Francesco S.,Wajchenberg Bernardo L.,Shuldiner Alan R.

Publisher

The Endocrine Society

Subject

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

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4. Genotype-phenotype correlations of Berardinelli-Seip congenital lipodystrophy and novel candidate genes prediction;Orphanet Journal of Rare Diseases;2020-04-29

5. Leu124Serfs*26, a novel AGPAT2 mutation in congenital generalized lipodystrophy with early cardiovascular complications;Diabetology & Metabolic Syndrome;2020-04-06