Point mutations in the growth hormone receptor gene of patients with Laron syndrome
Acta Paediatr Suppl
.
1992 Sep:383:132-3.
Authors
S Amselem
1
,
B Duriez
,
M L Sobrier
,
P Duquesnoy
,
M Goossens
Affiliation
1
Laboratory of Molecular Genetics, INSERM U 91, Hôpital Henri Mondor, Créteil, France.
PMID:
1458008
No abstract available
Publication types
Research Support, Non-U.S. Gov't
Review
MeSH terms
Dwarfism / genetics*
Humans
Point Mutation*
Receptors, Somatotropin*
Syndrome
Substances
Receptors, Somatotropin