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Paper Details

Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasia.
Am J Hum Genet
22
2013
C12orf57, CCH, amino acid, c12orf57, cerebral commissure, conserved gene, corpus callosum hypoplasia, genetic syndromes, human, initiator methionine codon, methionine, paralogs, recessive corpus callosum hypoplasia, syndromic
Author NameAffiliation
Naiara AkizuHoward Hughes Medical Institute, University of California
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