Unusual Phenotypic Features in a Patient with a Novel Splice Mutation in the GHRHR Gene

Isolated growth hormone deficiency (IGHD) may be of genetic origin. One of the few genes involved in that condition encodes the growth hormone releasing hormone receptor (GHRHR) that, through its ligand (GHRH), plays a pivotal role in the GH synthesis and secretion by the pituitary. Our objective is...

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Detalhes bibliográficos
Main Authors: Hilal, Latifa, Hajaji, Yassir, Vie-Luton, Marie-Pierre, Ajaltouni, Zeina, Benazzouz, Bouchra, Chana, Maha, Chraïbi, Adelmajid, Kadiri, Abdelkrim, Amselem, Serge, Sobrier, Marie-Laure
Formato: Artigo
Idioma:Inglês
Publicado em: ScholarOne 2008
Assuntos:
Research Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2249753/
https://ncbi.nlm.nih.gov/pubmed/18297129
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2119/2007-00128.Hilal
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