Home LiteratureArticle Details
PMID: 9500540 Published · ppublish English Case Reports News Research Support, Non-U.S. Gov't

A leptin missense mutation associated with hypogonadism and morbid obesity.

Nature genetics ·Vol. 18 ·No. 3 ·1998-03-00 ·Pages 213-5

Strobel A, Issad T, Camoin L, Ozata M, Strosberg AD

Abstract

暂无摘要

MeSH Terms
Adolescent Adult Animals COS Cells Child Chorionic Gonadotropin/pharmacology Female Homozygote Humans Hydrocortisone/blood Hypogonadism/drug therapy,genetics Insulin/blood Karyotyping Leptin Male Middle Aged Mutation Obesity, Morbid/genetics Pedigree Proteins/analysis,genetics Puberty/genetics Transfection
Chemicals
Chorionic Gonadotropin Insulin Leptin Proteins Hydrocortisone
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Strobel A
Issad T
Camoin L
Ozata M
Strosberg A D
Article Info
Journal
Nature genetics
Abbr.
Nat Genet
ISSN
1061-4036
DOI
10.1038/ng0398-213
Published
1998-03-00
Pages
213-5
Language
English
Region
United States
NLM ID
9216904
Subset
IM
External Links
PubMed source DOI: 10.1038/ng0398-213 View journal details
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]

Copyright © 2026.Genelibs Jinan Honghui Biotechnology Co., Ltd. 鲁ICP备20007159号-2