Literature DB >> 12519376

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

D Bönsch, C Neumann, R Lang-Roth, O Witte, A Lamprecht-Dinnesen, T Deufel.   

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Year:  2003        PMID： 12519376     DOI： 10.1034/j.1399-0004.2003.630112.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  3 in total

1.  A novel autosomal recessive nonsyndromic hearing impairment locus (DFNB42) maps to chromosome 3q13.31-q22.3.

Authors:  Muhammad Aslam; Muhammad Wajid; Maria H Chahrour; Muhammad Ansar; Sayedul Haque; Thanh L Pham; Regie P Santos; Kai Yan; Wasim Ahmad; Suzanne M Leal
Journal:  Am J Med Genet A       Date:  2005-02-15       Impact factor: 2.802

2.  [A new gene locus for an autosomal-dominant non-syndromic hearing impairment (DFNA 33) is situated on chromosome 13q34-qter].

Authors:  D Bönsch; C-M Schmidt; P Scheer; J Bohlender; C Neumann; A Am Zehnhoff-Dinnesen; T Deufel
Journal:  HNO       Date:  2009-04       Impact factor: 1.284

3.  [A new locus for an autosomal dominant, non-syndromic hearing impairment (DFNA57) located on chromosome 19p13.2 and overlapping with DFNB15].

Authors:  D Bönsch; C M Schmidt; P Scheer; J Bohlender; C Neumann; A am Zehnhoff-Dinnesen; T Deufel
Journal:  HNO       Date:  2008-02       Impact factor: 1.284
  3 in total

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