Rabson Mendenhall Syndrome caused by a novel missense mutation

BACKGROUND: Rabson Mendenhall syndrome is a rare endocrine condition characterized by severe insulin resistance and hyperglycemia. It occurs due to mutations in the insulin receptor gene. Few mutations which are associated with Rabson Mendenhall syndrome have been identified and reported in the past...

Descripción completa

Detalles Bibliográficos
Autores principales: Sinnarajah, Krishnapradeep, Dayasiri, M. B. K. C., Dissanayake, N. D. W., Kudagammana, S. T., Jayaweera, A. H. H. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5114824/
https://www.ncbi.nlm.nih.gov/pubmed/27891155
http://dx.doi.org/10.1186/s13633-016-0039-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5114824/
https://www.ncbi.nlm.nih.gov/pubmed/27891155
http://dx.doi.org/10.1186/s13633-016-0039-1

Ejemplares similares