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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
and HMX3 as candidate genes in hearing and vestibular function.
Pevsner et al.,
Baltimore, United States.
Am J Med Genet A
propose that hemizygous deletions of
and HMX3 are responsible for inner ear malformations, vestibular dysfunction, and congenital sensorineural hearing loss
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