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Original Article
Exome sequencing analysis reveals homozygous GJB2 gene mutation in a Mexican family with profound hearing loss
El análisis de secuenciacion del exoma identifica una mutación homocigota en el gen GJB2 en una familia mexicana con pérdida auditiva profunda
M. Martínez-Saucedoa, M.R. Rivera-Vegaa, L.M. Gonzalez-Huertaa, H. Urueta-Cuéllara, S.A. Cuevas-Covarrubiasa,b,
Corresponding author
sergiocuevasunam@gmail.com
sercuevas@yahoo.com

Corresponding author at: Dr. Balmis 148 Col. Doctores, C.P. 06726 México, D.F., Mexico.
a Servicio de Genética, Hospital General de México, Mexico City, Mexico
b Facultad de Medicina, Universidad Nacional Autónoma de México, Mexico City, Mexico
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ISSN: 01851063
Original language: English
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