Congenital stationary night blindness associated with mutations in GRM6 encoding glutamate receptor MGluR6

Những quyển sách tương tự

• Mutations in GRM6 identified in consanguineous Pakistani families with congenital stationary night blindness
  Bằng: Naeem, Muhammad Asif, et al.
  Được phát hành: (2015)
• Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6
  Bằng: Dryja, Thaddeus P., et al.
  Được phát hành: (2005)
• Identification of a new mutant allele, Grm6(nob7), for complete congenital stationary night blindness
  Bằng: QIAN, HAOHUA, et al.
  Được phát hành: (2015)
• Genotype-phenotype correlation in British families with X linked congenital stationary night blindness
  Bằng: Allen, L E, et al.
  Được phát hành: (2003)
• Restoration of mGluR6 Localization Following AAV-Mediated Delivery in a Mouse Model of Congenital Stationary Night Blindness
  Bằng: Varin, Juliette, et al.
  Được phát hành: (2021)