FANCC Dutch founder mutation in a Mennonite family from Tamaulipas, México

FANCC Dutch founder mutation in a Mennonite family from Tamaulipas, México

Abstract Background Fanconi anemia (FA) (OMIM #227650) is a rare hereditary disease characterized by genomic instability. The clinical phenotype involves malformations, bone marrow failure, and cancer predisposition. Genetic heterogeneity is a remarkable feature of FA; at least 22 FANC genes are kno...

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Bibliographic Details
Main Authors: Benilde García‐de Teresa, Sara Frias, Bertha Molina, María Teresa Villarreal, Alfredo Rodriguez, Alessandra Carnevale, Gerardo López‐Hernández, Lilia Vollbrechtshausen, Alberto Olaya‐Vargas, Leda Torres
Format: Article
Language:English
Published: Wiley 2019-06-01
Series:Molecular Genetics & Genomic Medicine
Subjects:
FANCC
FANCC c.67delG
fanconi anemia
Mennonite
Online Access:https://doi.org/10.1002/mgg3.710

Internet

https://doi.org/10.1002/mgg3.710

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