A large deletion in GPR98 causes type IIC Usher syndrome in male and female patients of an Iranian family

Lignende værker

• Two Iranian Families with a Novel Mutation in GJB2 Causing Autosomal Dominant Nonsyndromic Hearing Loss
  af: Bazazzadegan, Niloofar, et al.
  Udgivet: (2011)
• Investigating Seven Recently Identified Genes in 100 Iranian Families with Autosomal Recessive Non-syndromic Hearing Loss
  af: Reihaneh Alikhani, et al.
  Udgivet: (2015-09-01)
• A Novel Deletion Mutation in ASPM Gene in an Iranian Family with Autosomal Recessive Primary Microcephaly
  af: AKBARIAZAR, Elinaz, et al.
  Udgivet: (2013)
• A novel homozygous variant of GPR98 causes usher syndrome type IIC in a consanguineous Chinese family by next generation sequencing
  af: Wei, Chunli, et al.
  Udgivet: (2018)
• Domain analyses of Usher syndrome causing Clarin-1 and GPR98 protein models
  af: Khan, Sehrish Haider, et al.
  Udgivet: (2014)