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

Author:

D. Bahena-Bahena,J. López-Valdez,K. Raymond,R. Salinas-Marín,A. Ortega-García,B.G. Ng,H.H. Freeze,M. Ruíz-García,I. Martínez-Duncker

Publication:

Molecular Genetics and Metabolism Reports

Publisher:

Elsevier

Date:

2014

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