Open AccessBiallelic Mutations inCRB1Underlie Autosomal Recessive Familial Foveal Retinoschisis
Author(s) -
Ajoy Vincent,
Judith Ng,
Christina GerthKahlert,
Erika Tavares,
Jason T. Maynes,
Thomas Wright,
Amit K. Tiwari,
Anupreet Tumber,
Shuning Li,
James V. M. Hanson,
Angela Bahr,
H. Robson MacDonald,
Luzy Bähr,
Carol A. Westall,
Wolfgang Berger,
Frans P.M. Cremers,
Anneke I. den Hollander,
Elise Héon
Publication year - 2016
Publication title -
investigative ophthalmology and visual science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.935
H-Index - 218
eISSN - 1552-5783
pISSN - 0146-0404
DOI - 10.1167/iovs.15-18281
Subject(s) - genetics , biology , retinoschisis , electroretinography , exome sequencing , ophthalmology , phenotype , gene , retinal , medicine , retinal detachment , biochemistry
To identify the genetic cause of autosomal recessive familial foveal retinoschisis (FFR).
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