Mutations in the mitochondrial gene C12ORF65 lead to syndromic autosomal recessive intellectual disability and show genotype phenotype correlation

Published 2013 View Full Article

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Title
Mutations in the mitochondrial gene C12ORF65 lead to syndromic autosomal recessive intellectual disability and show genotype phenotype correlation
Authors
Keywords
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Journal
European Journal of Medical Genetics
Volume 56, Issue 11, Pages 599-602
Publisher
Elsevier BV
Online
2013-09-29
DOI
10.1016/j.ejmg.2013.09.010

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