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

Clinical endocrinology - 1 Aug 2020

Gorin Kobi, Golomb Mordechai, Spitzen Shoshi, Leitersdorf Eran, Schurr Daniel, Haj-Yahia Arin, Weiss Ram, Leibowitz Gil, Durst Ronen

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PMID: 32412105
DOI: 10.1111/cen.14223

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A rare frameshift mutation in the AGPAT2 gene in a family from gaza with congenital generalized lipodystrophy.PMID 32412105Read ↗

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