Mutations in TULP1, NR2E3, and MFRP genes in Indian families with autosomal recessive retinitis pigmentosa

Gelijkaardige items

• Genetic Analysis of Indian Families with Autosomal Recessive Retinitis Pigmentosa by Homozygosity Screening
  door: Singh, Hardeep Pal, et al.
  Gepubliceerd in: (2009)
• Mutation of SPATA7 in a family with autosomal recessive early-onset retinitis pigmentosa
  door: Kannabiran, Chitra, et al.
  Gepubliceerd in: (2012)
• Progress of gene research on autosomal recessive retinitis pigmentosa
  door: Rui Wang, et al.
  Gepubliceerd in: (2019-12-01)
• Homozygosity Mapping in Leber Congenital Amaurosis and Autosomal Recessive Retinitis Pigmentosa in South Indian Families
  door: Srilekha, Sundaramurthy, et al.
  Gepubliceerd in: (2015)
• RP1 mutations cause autosomal recessive retinitis pigmentosa
  Gepubliceerd in: (2005)