Exome sequencing analysis reveals homozygous GJB2 gene...

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Revista Médica Del Hospital General De México 2016 / 8

Exome sequencing analysis reveals homozygous GJB2 gene mutation in a Mexican family with profound hearing loss

Martínez-Saucedo, M., Rivera-Vega, M.R., Gonzalez-Huerta, L.M., Urueta-Cuellar, H., Cuevas-Covarrubias, S.
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Journal:
Revista Médica del Hospital General de México
DOI:
10.1016/j.hgmx.2016.08.001
Date:
August, 2016
File:
PDF, 710 KB
2016
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