ATP6V0A2 mutations present in two Mexican Mestizo children with an autosomal recessive cutis laxa syndrome type IIA.

Name: ATP6V0A2 mutations present in two Mexican Mestizo children with an autosomal recessive cutis laxa syndrome type IIA.
Author: Bahena-Bahena, D

ATP6V0A2 mutations present in two Mexican Mestizo children with an autosomal recessive cutis laxa syndrome type IIA. — المؤلف: Bahena-Bahena, D — Molecular genetics and metabolism reports 2014

المؤلف: Bahena-Bahena, D
النشر: Molecular genetics and metabolism reports 2014
الوصف: 203-212 p.