A rare frameshift mutation in the AGPAT2 gene in a family from gaza with congenital generalized lipodystrophy

Authors :: Gil Leibowitz
Daniel Schurr
Arin Haj‐Yahia
Ram Weiss
Eran Leitersdorf
Mordechai Golomb
Kobi Gorin
Ronen Durst
Shoshi Spitzen
Source :: Clinical Endocrinology. 93:212-214
Publication Year :: 2020
Publisher :: Wiley, 2020.

Subjects :: Genetics
medicine.medical_specialty
business.industry
Endocrinology, Diabetes and Metabolism
Hypertriglyceridemia
medicine.disease
Frameshift mutation
Congenital generalized lipodystrophy
Endocrinology
Internal medicine
Medicine
Lipodystrophy
business
Gene

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