A novel mutation in the leptin gene (W121X) in an Egyptian family

Congenital leptin deficiency is a rare recessively inherited condition due to homozygous mutations in the LEP gene. To date, only nine mutations have been identified in the LEP gene (p.L72S, p.N103K, p.R105W, p.H118L, p.S141C, c.104_106delTCA, c.135del3bp, c.398delG and c.481_482delCT). In this stud...

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Bibliographic Details
Published in:	Mol Genet Metab Rep
Main Authors:	Mazen, Inas, Amr, Khalda, Tantawy, Sally, Farooqi, I. Sadaf, El Gammal, Mona
Format:	Artigo
Language:	Inglês
Published:	Elsevier 2014
Subjects:	Short Communication
Online Access:	https://ncbi.nlm.nih.gov/pmc/articles/PMC5121350/ https://ncbi.nlm.nih.gov/pubmed/27896126 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgmr.2014.10.002
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A novel mutation in the leptin gene (W121X) in an Egyptian family

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