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Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndrome.
Liu XZ,
Hope C,
Walsh J,
Newton V,
Ke XM,
Liang CY,
Xu LR,
Zhou JM,
Trump D,
Steel KP,
Bundey S,
Brown SD.
PMID: 9718356 [PubMed - indexed for MEDLINE]
PMCID: PMC1377414
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Cited by 5 PubMed Central articles
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Usher syndrome type III: revised genomic structure of the USH3 gene and identification of novel mutations.
Fields RR, Zhou G, Huang D, Davis JR, Möller C, Jacobson SG, Kimberling WJ, Sumegi J.
Am J Hum Genet. 2002 Sep; 71(3):607-17. Epub 2002 Jul 16.
[Am J Hum Genet. 2002]
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ReviewAt the speed of sound: gene discovery in the auditory system.
Resendes BL, Williamson RE, Morton CC.
Am J Hum Genet. 2001 Nov; 69(5):923-35. Epub 2001 Sep 27.
[Am J Hum Genet. 2001]
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Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F.
Ahmed ZM, Riazuddin S, Bernstein SL, Ahmed Z, Khan S, Griffith AJ, Morell RJ, Friedman TB, Riazuddin S, Wilcox ER.
Am J Hum Genet. 2001 Jul; 69(1):25-34. Epub 2001 Jun 7.
[Am J Hum Genet. 2001]
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