249 related articles for article (PubMed ID: 16935610)
21. The manner of decay of genetically defective EYS gene transcripts in photoreceptor-directed fibroblasts derived from retinitis pigmentosa patients depends on the type of mutation.
Seko Y; Iwanami M; Miyamoto-Matsui K; Takita S; Aoi N; Umezawa A; Kato S
Stem Cell Res Ther; 2018 Oct; 9(1):279. PubMed ID: 30359287
[TBL] [Abstract][Full Text] [Related]
22. Abnormal distribution of red/green cone opsins in a patient with an autosomal dominant cone dystrophy.
Bonilha VL; Hollyfield JG; Grover S; Fishman GA
Ophthalmic Genet; 2005 Jun; 26(2):69-76. PubMed ID: 16020309
[TBL] [Abstract][Full Text] [Related]
23. Identification of an intronic single-point mutation in RP2 as the cause of semidominant X-linked retinitis pigmentosa.
Pomares E; Riera M; Castro-Navarro J; Andrés-Gutiérrez A; Gonzàlez-Duarte R; Marfany G
Invest Ophthalmol Vis Sci; 2009 Nov; 50(11):5107-14. PubMed ID: 19516003
[TBL] [Abstract][Full Text] [Related]
24. Two novel mutations of the retinitis pigmentosa GTPase regulator gene in two Chinese families with X-linked retinitis pigmentosa.
Liu L; Chen H; Liu M; Jin L; Wei Y; Wu X; Liu Y; Xhu R; Chai J
Chin Med J (Engl); 2002 Jun; 115(6):833-6. PubMed ID: 12123547
[TBL] [
