PROMM and deafness: exclusion of ZNF9 as the disease gene in DFNA18 suggests a polygenic origin of the PROMM/DM2 phenotype

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Bibliographic Details
Published in:Clinical genetics 2003-01, Vol.63 (1), p.73-75
Main Authors: Bönsch, D, Neumann, C, Lang-Roth, R, Witte, O, Lamprecht-Dinnesen, A, Deufel, T
Format: Article
Language:English
Subjects:
Chromosome Mapping
Chromosomes, Human, Pair 3
Deafness - genetics
Humans
Myotonic Disorders - genetics
Myotonin-Protein Kinase
Protein-Serine-Threonine Kinases - genetics
RNA-Binding Proteins - genetics
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ISSN:0009-9163
1399-0004
DOI:10.1034/j.1399-0004.2003.630112.x