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PubMed (OMIM) for id: 340051
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PROMM and deafness: exclusion of ZNF9 as the disease gene in DFNA18 suggests a polygenic origin of the PROMM/DM2 phenotype.
Clin Genet. 2003 Jan;63(1):73-5. doi: 10.1034/j.1399-0004.2003.630112.x.
Clin Genet. 2003.
PMID: 12519376
No abstract available.
A novel locus for autosomal dominant, non-syndromic hearing impairment (DFNA18) maps to chromosome 3q22 immediately adjacent to the DM2 locus.
Bönsch D, Scheer P, Neumann C, Lang-Roth R, Seifert E, Storch P, Weiller C, Lamprecht-Dinnesen A, Deufel T.
Bönsch D, et al.
Eur J Hum Genet. 2001 Mar;9(3):165-70. doi: 10.1038/sj.ejhg.5200612.
Eur J Hum Genet. 2001.
PMID: 11313754
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