Identification of two mutations of the RHO gene in two Chinese families with retinitis pigmentosa: Correlation between genotype and phenotype

Схожие документы

• Large novel deletions detected in Chinese families with aniridia: correlation between genotype and phenotype
  по: Zhang, Xiaohui, et al.
  Опубликовано: (2011)
• Novel Mutations of RPGR in Chinese Retinitis Pigmentosa Patients and the Genotype-Phenotype Correlation
  по: Yang, Liping, et al.
  Опубликовано: (2014)
• Phenotype-genotype correlations in autosomal dominant retinitis pigmentosa caused by RHO, D190N
  по: Tsui, Irena, et al.
  Опубликовано: (2008)
• Phenotype-genotype correlations in X linked retinitis pigmentosa.
  по: Kaplan, J, et al.
  Опубликовано: (1992)
• Two novel PRPF31 premessenger ribonucleic acid processing factor 31 homolog mutations including a complex insertion-deletion identified in Chinese families with retinitis pigmentosa
  по: Dong, Bing, et al.
  Опубликовано: (2013)