Novel TMPRSS3 variants in Pakistani families with autosomal recessive nonsyndromic hearing impairment

Lignende værker

• A Novel ESRRB Deletion Is a Rare Cause of Autosomal Recessive Nonsyndromic Hearing Impairment among Pakistani Families
  af: Lee, Kwanghyuk, et al.
  Udgivet: (2011)
• Autosomal Recessive Nonsyndromic Hearing Impairment due to a Novel Deletion in the RDX Gene
  af: Lee, Kwanghyuk, et al.
  Udgivet: (2011)
• Novel CLDN14 Mutations in Pakistani Families With Autosomal Recessive Non-Syndromic Hearing Loss
  af: Lee, Kwanghyuk, et al.
  Udgivet: (2012)
• Splice-site mutations in the TRIC gene underlie autosomal recessive nonsyndromic hearing impairment in Pakistani families
  af: Chishti, Muhammad S., et al.
  Udgivet: (2007)
• Novel Autosomal Recessive Nonsyndromic Hearing Impairment Locus DFNB90 Maps to 7p22.1-p15.3
  af: Ali, Ghazanfar, et al.
  Udgivet: (2011)