Characterization of the human growth hormone receptor gene and demonstration of a partial gene deletion in two patients with Laron-type dwarfism.

Laron-type dwarfism is an autosomal recessive genetic disorder that is characterized by high levels of growth hormone and low levels of insulin-like growth factor I in the circulation. Several lines of evidence suggest that this disease is caused by a defect in the growth hormone receptor. In order...

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Pubblicato in:	Proc Natl Acad Sci U S A
Autori principali:	Godowski, P J, Leung, D W, Meacham, L R, Galgani, J P, Hellmiss, R, Keret, R, Rotwein, P S, Parks, J S, Laron, Z, Wood, W I
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	National Academy of Sciences 1989
Soggetti:	Research Article
Accesso online:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC298219/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2813379/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.86.20.8083
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