A leptin missense mutation associated with hypogonadism and morbid obesity

Nature Genetics

Volumn 18, Issue 3, 1998, Pages 214-215

  Strobel, Andreas ^a,b   Issad, Tarik ^a   Camoin, Luc ^a   Ozata, Metin ^c   Strosberg, A Donny ^a  

^a CNRS   (France)

^b JOHANNES GUTENBERG UNIVERSITY   (Germany)

^c GULHANE SCHOOL OF MEDICINE   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

CHORIONIC GONADOTROPIN; HYDROCORTISONE; INSULIN; LEPTIN; PROTEIN;

ADOLESCENT; ADULT; ANIMAL; ARTICLE; BLOOD; CASE REPORT; CELL STRAIN COS1; CHILD; FEMALE; GENETIC TRANSFECTION; GENETICS; HOMOZYGOTE; HUMAN; HYPOGONADISM; KARYOTYPING; MALE; MIDDLE AGED; MORBID OBESITY; MUTATION; PEDIGREE; PUBERTY;

ADOLESCENT; ADULT; ANIMALS; CHILD; CHORIONIC GONADOTROPIN; COS CELLS; FEMALE; HOMOZYGOTE; HUMANS; HYDROCORTISONE; HYPOGONADISM; INSULIN; KARYOTYPING; LEPTIN; MALE; MIDDLE AGED; MUTATION; OBESITY, MORBID; PEDIGREE; PROTEINS; PUBERTY; TRANSFECTION;

EID: 0032014836     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng0398-213     Document Type: Letter

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