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Items: 7

1.

Mapping of a novel locus for achromatopsia (ACHM4) to 1p and identification of a germline mutation in the alpha subunit of cone transducin (GNAT2).

Aligianis IA, Forshew T, Johnson S, Michaelides M, Johnson CA, Trembath RC, Hunt DM, Moore AT, Maher ER.

J Med Genet. 2002 Sep;39(9):656-60.

2.

Achromatopsia: a review.

Remmer MH, Rastogi N, Ranka MP, Ceisler EJ.

Curr Opin Ophthalmol. 2015 Jul;26(5):333-40. doi: 10.1097/ICU.0000000000000189. Review.

PMID:
26196097
3.

[Genetics of congenital color vision defects. II. Rare types of color blindness].

Krawczyński MR.

Klin Oczna. 1995 Jan-Feb;97(1-2):39-43. Review. Polish.

PMID:
7637312
4.

[Progress on study of achromatopsia and targeted gene therapy].

Dai XF, Pang JJ.

Zhonghua Yan Ke Za Zhi. 2012 Aug;48(8):755-8. Review. Chinese.

PMID:
23141518
5.

[Genetic causes of hereditary cone and cone-rod dystrophies].

Kohl S.

Ophthalmologe. 2009 Feb;106(2):109-15. doi: 10.1007/s00347-008-1864-2. Review. German.

PMID:
19184602
6.


Gene Therapy for Color Blindness.

Hassall MM, Barnard AR, MacLaren RE.

Yale J Biol Med. 2017 Dec 19;90(4):543-551. eCollection 2017 Dec. Review.

7.

[Achromatopsia].

Poloschek CM, Kohl S.

Ophthalmologe. 2010 Jun;107(6):571-80; quiz 581-2. doi: 10.1007/s00347-010-2178-8. Review. German.

PMID:
20533046

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