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...

Celý popis

Uloženo v:
Podrobná bibliografie
Hlavní autoři: Mohamadi, Ali, Martari, Marco, Holladay, Cindy D., Phillips, John A., Mullis, Primus E., Salvatori, Roberto
Médium: Artigo
Jazyk:Inglês
Vydáno: The Endocrine Society 2009
Témata:
Original Article
On-line přístup: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
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky