ATP6V0A2 mutations present in two Mexican Mestizo children with an autosomal recessive cutis laxa syndrome type IIA.
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ATP6V0A2 mutations present in two Mexican Mestizo children with an autosomal recessive cutis laxa syndrome type IIA.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 25 April 2014
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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name
ATP6V0A2 mutations present in ...... cutis laxa syndrome type IIA.
@en
ATP6V0A2 mutations present in ...... cutis laxa syndrome type IIA.
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type
label
ATP6V0A2 mutations present in ...... cutis laxa syndrome type IIA.
@en
ATP6V0A2 mutations present in ...... cutis laxa syndrome type IIA.
@nl
prefLabel
ATP6V0A2 mutations present in ...... cutis laxa syndrome type IIA.
@en
ATP6V0A2 mutations present in ...... cutis laxa syndrome type IIA.
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P2093
P2860
P50
P1476
ATP6V0A2 mutations present in ...... cutis laxa syndrome type IIA.
@en
P2093
A Ortega-García
D Bahena-Bahena
J López-Valdez
M Ruíz-García
P2860
P304
P356
10.1016/J.YMGMR.2014.04.003
P577
2014-04-25T00:00:00Z