2004

  • Mohiddin SA, Ahmed ZM, Griffith AJ, Tripodi D, Friedman TB, Fananapazir L, Morell RJ. (2004)
  • Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in Unconventional Myosin VI (MYO6).
  • J Med Genet 41(4):309-314
  • Ahmed ZM, Li XC, Powell SD, Riazuddin S, Young TL, Ramzan K, Ahmad Z, Luscombe S, Dhillon K, MacLaren L, Ploplis B, Shotland LI, Ives E, Riazuddin S, Friedman TB, Morell RJ, Wilcox ER. (2004)
  • Characterization of a new full-length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan.
  • BMC Med Genet 5:24
  • Naz S, Griffith AJ, Riazuddin S, Hampton LL, Battey JF, Riazuddin, S, Wilcox ER, Friedman TB. (2004)
  • Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction.
  • J Med Genet 40:360-63