FANCC Dutch founder mutation in a Mennonite family from Tamaulipas, M éxico

ConclusionThe identification of theFANCC c.67delG mutation in this family not only allows proper genetic counseling, but it also grants the possibility to raise awareness of FA risk among the Mennonite community living in Mexico.

Source: Molecular Genetics & Genomic Medicine - April 30, 2019 Category: Genetics & Stem Cells Authors: Benilde Garc ía‐de Teresa, Sara Frias, Bertha Molina, María Teresa Villarreal, Alfredo Rodriguez, Alessandra Carnevale, Gerardo López‐Hernández, Lilia Vollbrechtshausen, Alberto Olaya‐Vargas, Leda Torres Tags: CLINICAL REPORT Source Type: research