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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 08 Dec 2016.

H6 homeobox 2

Hmx2, H6L, Nkx5-2, Nkx5.2
Papers on Hmx2
Molecular (SNP) analyses of overlapping hemizygous deletions of 10q25.3 to 10qter in four patients: evidence for HMX2 and HMX3 as candidate genes in hearing and vestibular function.
GeneRIF
Pevsner et al., Baltimore, United States. In Am J Med Genet A, 2009
propose that hemizygous deletions of HMX2 and HMX3 are responsible for inner ear malformations, vestibular dysfunction, and congenital sensorineural hearing loss
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