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Browsing by Author Ahmed, Z.M.

Full Text	Issue Date	Title	Author(s)
	2008	Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome.	Ahmed, Z.M.; Riazuddin, Saima; Aye, S.; Ali, R.A.; Venselaar, H., et al
	2008	Mutations of ESRRB encoding estrogen-related receptor beta cause autosomal-recessive nonsyndromic hearing impairment DFNB35.	Collin, R.W.J.; Kalay, E.; Tariq, M.; Peters, T.A.; Zwaag, B. van der, et al
	2008	Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.	Ahmed, Z.M.; Masmoudi, S.; Kalay, E.; Belyantseva, I.A.; Mosrati, M.A., et al