MON-LB014 Autosomal Dominant Growth Hormone Deficiency Due to a Novel c.178g>A Mutation in the GH1 Gene Is Caused by Alternative Splicing to Produce a Small GH Isoform

Introduction: Growth hormone (GH) plays a vital role in human physiology. Mutations in GH1 cause isolated growth hormone deficiency (GHD). The most frequent cause of familial growth hormone deficiency is Type II autosomal dominant GHD (isolated GHD type II) due to several heterozygous GH1 mutations....

Descripción completa

Detalles Bibliográficos
Autores principales: Miller, Bradley Scott, Rihs, Silvia, Parween, Shaheena, Ternand, Christine, Gregory, Louise Cheryl, Dattani, Mehul Tulsidas, Pandey, Amit V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Pediatric Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7209589/
http://dx.doi.org/10.1210/jendso/bvaa046.2187

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7209589/
http://dx.doi.org/10.1210/jendso/bvaa046.2187

Ejemplares similares