Identification of a novel mutation in CRYM in a Chinese family with hearing loss using whole-exome sequencing

Eitemau Tebyg

• Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing
  gan: Woo, Hae-Mi, et al.
  Cyhoeddwyd: (2014)
• Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families
  gan: Zhou, Yingjie, et al.
  Cyhoeddwyd: (2020)
• Identification of a novel mutation in a Chinese family with Nance-Horan syndrome by whole exome sequencing
  gan: Hong, Nan, et al.
  Cyhoeddwyd: (2014)
• Whole-Exome Sequencing to Decipher the Genetic Heterogeneity of Hearing Loss in a Chinese Family with Deaf by Deaf Mating
  gan: Qing, Jie, et al.
  Cyhoeddwyd: (2014)
• Erratum to: Identification of a novel mutation in a Chinese family with Nance-Horan syndrome by whole exome sequencing
  gan: Hong, Nan, et al.
  Cyhoeddwyd: (2014)