ABCA4 c.6282+3A>T

Variant ID: 1-94467411-T-A

NM_000350.2(ABCA4):c.6282+3A>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Extensive genic and allelic heterogeneity underlying inherited retinal dystrophies in Mexican patients molecularly analyzed by next-generation sequencing.

Molecular Genetics & Genomic Medicine
Zenteno, Juan C JC; García-Montaño, Leopoldo A LA; Cruz-Aguilar, Marisa M; Ronquillo, Josué J; Rodas-Serrano, Agustín A; Aguilar-Castul, Luis L; Matsui, Rodrigo R; Vencedor-Meraz, Carlos I CI; Arce-González, Rocío R; Graue-Wiechers, Federico F; Gutiérrez-Paz, Mario M; Urrea-Victoria, Tatiana T; de Dios Cuadras, Ulises U; Chacón-Camacho, Oscar F OF
Publication Date: 2020-01

Variant appearance in text: ABCA4: 6282+3A>T
PubMed Link: 31736247
Variant Present in the following documents:
  • Main text
  • MGG3-8-0-s001.pdf
  • MGG3-8-0.pdf
View BVdb publication page