Ancient founder mutation is responsible for Imerslund-Gräsbeck Syndrome among diverse ethnicities

BACKGROUND: Imerslund-Gräsbeck syndrome (IGS) was described just over 50 years ago by Olga Imerslund and Ralph Gräsbeck and colleagues. IGS is caused by specific malabsorption of cobalamin (Cbl) due to bi-allelic mutations in either the cubilin gene (CUBN) or the human amnionless homolog (AMN). Muta...

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Detalles Bibliográficos
Autores principales: Beech, Cameron M, Liyanarachchi, Sandya, Shah, Nidhi P, Sturm, Amy C, Sadiq, May F, de la Chapelle, Albert, Tanner, Stephan M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3226546/
https://www.ncbi.nlm.nih.gov/pubmed/22078000
http://dx.doi.org/10.1186/1750-1172-6-74

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3226546/
https://www.ncbi.nlm.nih.gov/pubmed/22078000
http://dx.doi.org/10.1186/1750-1172-6-74

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