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Summary Anatomy Item Literature (441) Expression Attributions Wiki
XB-ANAT-190

Papers associated with inner ear (and kcnj10)

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RNA-Seq and microarray analysis of the Xenopus inner ear transcriptome discloses orthologous OMIM(®) genes for hereditary disorders of hearing and balance., Ramírez-Gordillo D., BMC Res Notes. November 18, 2015; 8 691.      

KCNJ10 mutations display differential sensitivity to heteromerisation with KCNJ16., Parrock S., Nephron Physiol. January 1, 2013; 123 (3-4): 7-14.          

Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations., Bockenhauer D., N Engl J Med. May 7, 2009; 360 (19): 1960-70.

Mutations of KCNJ10 together with mutations of SLC26A4 cause digenic nonsyndromic hearing loss associated with enlarged vestibular aqueduct syndrome., Yang T., Am J Hum Genet. May 1, 2009; 84 (5): 651-7.      

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