Photoreceptor Progenitor mRNA Analysis Reveals Exon Skipping Resulting from the ABCA4 c.5461-10T→C Mutation in Stargardt Disease-Reference-Cited by-同舟云学术

Photoreceptor Progenitor mRNA Analysis Reveals Exon Skipping Resulting from the ABCA4 c.5461-10T→C Mutation in Stargardt Disease

Published:2016-06 Issue:6 Volume:123 Page:1375-1385
ISSN:0161-6420
Container-title:Ophthalmology
language:en
Short-container-title:Ophthalmology

Author:

Sangermano Riccardo,Bax Nathalie M.,Bauwens Miriam,van den Born L. Ingeborgh,De Baere Elfride,Garanto Alejandro,Collin Rob W.J.,Goercharn-Ramlal Angelique S.A.,den Engelsman-van Dijk Anke H.A.,Rohrschneider Klaus,Hoyng Carel B.,Cremers Frans P.M.,Albert Silvia^ORCID

Publisher

Elsevier BV

Subject

Ophthalmology

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3. A comprehensive survey of sequence variation in the ABCA4 (ABCR) gene in Stargardt disease and age-related macular degeneration;Rivera;Am J Hum Genet,2000

4. An analysis of allelic variation in the ABCA4 gene;Webster;Invest Ophthalmol Vis Sci,2001

5. A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy;Allikmets;Nat Genet,1997

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