Clinical and electroretinographic comparison between Åland Island eye disease and a newly found related disease with X-chromosomal inheritance-Reference-Cited by-同舟云学术

Clinical and electroretinographic comparison between Åland Island eye disease and a newly found related disease with X-chromosomal inheritance

Published:2009-05-27 Issue:6 Volume:69 Page:703-710
ISSN:1755-375X
Container-title:Acta Ophthalmologica
language:en
Short-container-title:

Author:

Carlson S.,Vesti E.,Raitta C.,Donner M.,Eriksson A. W.,Forsius H.

Publisher

Wiley

Subject

Ophthalmology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1755-3768.1991.tb02047.x/fullpdf

Reference13 articles.

1. Localization of the Åland Island eye disease locus to the pericentromeric region of the X chromosome by linkage analysis;Alitalo;Am J Hum Genet,1991

2. A DC electroretinography method for the recording of human a-, b- and c-waves;Carlson;J Neurosci Methods,1990

3. Ein neues Augensyndrom mit X-chromosomaler Transmission. Ein Sippe mit Fundusabinismus, Foveahypoplasie, Nystagmus, Myopie, Astigmatismus und Dyschromatopsie;Forsius;Klin Monatsbl. Augenheilkd,1964

4. The influence of cone adaptation upon rod mediated flicker;Fumkes;Vision Res,1986

5. Tonic inhibition of rod flicker by dark-adapted cones;Goldberg;Invest Ophthalmol Vis Sci (Suppl),1985

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1. A Novel Splice-Site Variant in CACNA1F Causes a Phenotype Synonymous with Åland Island Eye Disease and Incomplete Congenital Stationary Night Blindness;Genes;2021-01-27

2. Thirty distinct CACNA1F mutations in 33 families with incomplete type of XLCSNB and Cacna1f expression profiling in mouse retina;European Journal of Human Genetics;2002-07-16