TY  - GEN
AU  - Clément,K
AU  - Vaisse,C
AU  - Lahlou,N
AU  - Cabrol,S
AU  - Pelloux,V
AU  - Cassuto,D
AU  - Gourmelen,M
AU  - Dina,C
AU  - Chambaz,J
AU  - Lacorte,J M
AU  - Basdevant,A
AU  - Bougnères,P
AU  - Lebouc,Y
AU  - Froguel,P
AU  - Guy-Grand,B
TI  - A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction
SN  - 0028-0836
PY  - 1998///0416
KW  - Adult
KW  - Body Height
KW  - Body Weight
KW  - Carrier Proteins
KW  - genetics
KW  - Family Health
KW  - Female
KW  - Genotype
KW  - Homozygote
KW  - Human Growth Hormone
KW  - metabolism
KW  - Humans
KW  - Male
KW  - Mutation
KW  - Obesity
KW  - Pituitary Diseases
KW  - Polymorphism, Single-Stranded Conformational
KW  - RNA, Messenger
KW  - Receptors, Cell Surface
KW  - Receptors, Leptin
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1038/32911
ER  -