Identification and characterisation of a novel GHR defect disrupting the polypyrimidine tract and resulting in GH insensitivity

OBJECTIVE: GH insensitivity (GHI) is caused in the majority of cases by impaired function of the GH receptor (GHR). All but one known GHR mutation are in the coding sequence or the exon/intron boundaries. We identified and characterised the first intronic defect occurring in the polypyrimidine tract...

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Detalles Bibliográficos
Autores principales: David, A, Miraki-Moud, F, Shaw, N J, Savage, M O, Clark, A J L, Metherell, L A
Formato: Texto
Lenguaje:English
Publicado: BioScientifica 2010
Materias:
Clinical Study
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2792980/
https://www.ncbi.nlm.nih.gov/pubmed/19812236
http://dx.doi.org/10.1530/EJE-09-0583

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2792980/
https://www.ncbi.nlm.nih.gov/pubmed/19812236
http://dx.doi.org/10.1530/EJE-09-0583

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