Literature DB >> 8220430

Mutations of PAX3 unlikely in Waardenburg syndrome type 2.

S Arias.   

Abstract

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Year:  1993        PMID： 8220430     DOI： 10.1038/ng0993-8a

Source DB:  PubMed          Journal:  Nat Genet        ISSN： 1061-4036            Impact factor:   38.330


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  2 in total

1.  [Unilateral sensineural deafness associated with mutations in the PAX3-gene in Waardenburg syndrome type I].

Authors:  M Ptok; S Morlot
Journal:  HNO       Date:  2006-07       Impact factor: 1.284

2.  Further elucidation of the genomic structure of PAX3, and identification of two different point mutations within the PAX3 homeobox that cause Waardenburg syndrome type 1 in two families.

Authors:  A K Lalwani; J R Brister; J Fex; K M Grundfast; B Ploplis; T B San Agustin; E R Wilcox
Journal:  Am J Hum Genet       Date:  1995-01       Impact factor: 11.025
  2 in total

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