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A mutation in PDS causes non-syndromic recessive deafness.
PMID: 9500541 [PubMed - indexed for MEDLINE]
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Cited by 9 PubMed Central articles
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Transcriptional control of SLC26A4 is involved in Pendred syndrome and nonsyndromic enlargement of vestibular aqueduct (DFNB4).
Yang T, Vidarsson H, Rodrigo-Blomqvist S, Rosengren SS, Enerback S, Smith RJ.
Am J Hum Genet. 2007 Jun; 80(6):1055-63. Epub 2007 Apr 23.
[Am J Hum Genet. 2007]
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ReviewGenetic factors that might lead to different responses in individuals exposed to perchlorate.
Scinicariello F, Murray HE, Smith L, Wilbur S, Fowler BA.
Environ Health Perspect. 2005 Nov; 113(11):1479-84.
[Environ Health Perspect. 2005]
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A new locus for nonsyndromic deafness DFNB51 maps to chromosome 11p13-p12.
Shaikh RS, Ramzan K, Nazli S, Sattar S, Khan SN, Riazuddin S, Ahmed ZM, Friedman TB, Riazuddin S.
Am J Med Genet A. 2005 Nov 1; 138(4):392-5.
[Am J Med Genet A. 2005]
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