Mutation Analysis of the Muscarinic Cholinergic Receptor Genes in Isolated Growth Hormone Deficiency Type IB

Background: Isolated GH deficiency (IGHD) is familial in 5–30% of patients. The most frequent form (IGHD-IB) has autosomal recessive inheritance, and it is known that it can be caused by mutations in the GHRH receptor (GHRHR) gene or in the GH gene. However, most forms of IGHD-IB have an unknown gen...

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Detalhes bibliográficos
Main Authors: Mohamadi, Ali, Martari, Marco, Holladay, Cindy D., Phillips, John A., Mullis, Primus E., Salvatori, Roberto
Formato: Artigo
Idioma:Inglês
Publicado em: The Endocrine Society 2009
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2708943/
https://ncbi.nlm.nih.gov/pubmed/19417035
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2009-0512
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