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Results: 14

Related Articles by Review for PubMed (Select 8202715)

1.

Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci.

Kajiwara K, Berson EL, Dryja TP.

Science. 1994 Jun 10;264(5165):1604-8.

PMID:
8202715
2.

Role of subunit assembly in autosomal dominant retinitis pigmentosa linked to mutations in peripherin 2.

Molday RS, Molday LL, Loewen CJ.

Novartis Found Symp. 2004;255:95-112; discussion 113-6, 177-8. Review.

PMID:
14750599
3.
4.

[Candidate gene approach].

Hotta Y, Fujiki K.

Tanpakushitsu Kakusan Koso. 1996 Nov;41(15 Suppl):2433-40. Review. Japanese. No abstract available.

PMID:
8952407
5.

[A molecular biological study on retinitis pigmentosa].

Nakazawa M.

Nihon Ganka Gakkai Zasshi. 1993 Dec;97(12):1394-405. Review. Japanese.

PMID:
7904791
6.

Update on the molecular genetics of retinitis pigmentosa.

Wang Q, Chen Q, Zhao K, Wang L, Wang L, Traboulsi EI.

Ophthalmic Genet. 2001 Sep;22(3):133-54. Review.

PMID:
11559856
7.

[Retinitis pigmentosa--clinical, genetic and pathophysiologic aspects].

Jurklies B, Zrenner E, Wessing A.

Klin Monbl Augenheilkd. 1997 Jan;210(1):1-18. Review. German.

PMID:
9206727
8.

[Molecular pathology of retinitis pigmentosa].

Ohguro H, Maeda T, Yanagihashi S, Miyakawa Y, Maruyama I, Nakazawa M.

Nihon Ganka Gakkai Zasshi. 2002 Aug;106(8):461-73. Review. Japanese.

PMID:
12229196
9.

[Molecular-genetic basis of tapetoretinal degeneration].

Dzhemileva LU, Grinberg ER, Tazetdinov AM, Zaĭĭdullin IS, Bibkov MM, Musina VV, Khusnutdinova EK.

Mol Biol (Mosk). 2008 Jan-Feb;42(1):3-11. Review. Russian.

PMID:
18389614
10.

Identification of the RP1 and RP10 (IMPDH1) genes causing autosomal dominant RP.

Daiger SP, Sullivan LS, Bowne SJ, Kennan A, Humphries P, Birch DG, Heckenlively JR; RP1 Consortium.

Adv Exp Med Biol. 2003;533:1-11. Review. No abstract available.

11.

[Cause of retinitis pigmentosa and new therapeutics under development].

Sakamoto K, Mori A, Nakahara T, Ishii K.

Nihon Yakurigaku Zasshi. 2011 Jan;137(1):22-6. Review. Japanese. No abstract available.

PMID:
21233585
12.

[Molecular genetics of pigmentary retinopathy].

Millán JM, Nájera C, Beneyto M.

Med Clin (Barc). 1994 Jan 15;102(1):30-2. Review. Spanish. No abstract available.

PMID:
8133683
13.

Molecular heterogeneity in retinitis pigmentosa. More mutations.

Goldberg MF.

Ophthalmic Genet. 1994 Jun;15(2):47-50. Review. No abstract available.

PMID:
7850268
14.

Digenic inheritance in medical genetics.

Schäffer AA.

J Med Genet. 2013 Oct;50(10):641-52. doi: 10.1136/jmedgenet-2013-101713. Epub 2013 Jun 19. Review.

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