Correction (DOI:10.1016/j.ajo.2007.03.025);Novel Mutations in the GRK1 Gene in Japanese Patients With Oguchi Disease

American Journal of Ophthalmology

Volumn 144, Issue 3, 2007, Pages 475-477

  Oishi, Akio ^a   Akimoto, Masayuki ^a   Kawagoe, Naoaki ^a   Mandai, Michiko ^a   Takahashi, Masayo ^a   Yoshimura, Nagahisa ^a  

^a KYOTO UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

G PROTEIN COUPLED RECEPTOR KINASE; G PROTEIN COUPLED RECEPTOR KINASE 1; RETINA S ANTIGEN; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; ARTICLE; CASE REPORT; ELECTRORETINOGRAM; FEMALE; GENE MUTATION; GENE SEQUENCE; GENETIC CODE; HUMAN; JAPANESE; NULL ALLELE; OGUCHI DISEASE; PRIORITY JOURNAL;

EID: 34548237338     PISSN: 00029394     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ajo.2007.09.011     Document Type: Erratum

References (5)

1. Yamamoto S., Sippel K.C., Berson E.L., and Dryja T.P. Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness. Nat Genet 15 (1997) 175-178
2. Yamada T., Matsumoto M., Kadoi C., et al. 1147 del A mutation in the Arestin gene in Japanese patients with Oguchi disease. Ophthalmic Genet 20 (1999) 117-120
3. Saga M., Mashima Y., Kudoh J., Oguchi Y., and Shimizu N. Gene analysis and evaluation of the single founder effect in Japanese patients with Oguchi disease. Jpn J Ophthalmol 48 (2004) 350-352
4. Hayashi T., Gekka T., Takeuchi T., Goto-Omoto S., and Kitahara K. A novel homozygous GRK1 mutation (P391H) in 2 siblings with Oguchi disease with markedly reduced cone responses. Ophthalmology 114 (2007) 134-141
5. Cideciyan A.V., Zhao X., Nielsen L., et al. Null mutation in the rhodopsin kinase gene slows recovery kinetics of rod and cone phototransduction in man. Proc Natl Acad Sci U S A 95 (1998) 328-333