ABCA4 c.6280_6282del ;(p.L2094del)

Variant ID: 1-94467413-CCAG-C

NM_000350.2(ABCA4):c.6280_6282del;(p.L2094del)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Using single molecule Molecular Inversion Probes as a cost-effective, high-throughput sequencing approach to target all genes and loci associated with macular diseases.

Human Mutation
Hitti-Malin, Rebekkah J RJ; Dhaenens, Claire-Marie CM; Panneman, Daan M DM; Corradi, Zelia Z; Khan, Mubeen M; den Hollander, Anneke I AI; Farrar, G Jane GJ; Gilissen, Christian C; Hoischen, Alexander A; van de Vorst, Maartje M; Bults, Femke F; Boonen, Erica G M EGM; Saunders, Patrick P; , ; Roosing, Susanne S; Cremers, Frans P M FPM
Publication Date: 2022-10-19

Variant appearance in text: ABCA4: Leu2094del
PubMed Link: 36259723
Variant Present in the following documents:
  • HUMU-43-2234-s012.xlsx, sheet 1
  • HUMU-43-2234-s007.xlsx, sheet 1
View BVdb publication page



Clinical spectrum, genetic complexity and therapeutic approaches for retinal disease caused by ABCA4 mutations.

Progress In Retinal And Eye Research
Cremers, Frans P M FPM; Lee, Winston W; Collin, Rob W J RWJ; Allikmets, Rando R
Publication Date: 2020-11

Variant appearance in text: ABCA4: Leu2094del
PubMed Link: 32278709
Variant Present in the following documents:
  • Main text
  • nihms-1627942.pdf
View BVdb publication page