USH2A c.11357del ;(p.P3786Lfs*6)

Variant ID: 1-215931968-AG-A

NM_206933.2(USH2A):c.11357del;(p.P3786Lfs*6)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Unraveling the genetic complexities of combined retinal dystrophy and hearing impairment.

Human Genetics
Bahena, Paulina P; Daftarian, Narsis N; Maroofian, Reza R; Linares, Paola P; Villalobos, Daniel D; Mirrahimi, Mehraban M; Rad, Aboulfazl A; Doll, Julia J; Hofrichter, Michaela A H MAH; Koparir, Asuman A; Röder, Tabea T; Han, Seungbin S; Sabbaghi, Hamideh H; Ahmadieh, Hamid H; Behboudi, Hassan H; Villanueva-Mendoza, Cristina C; Cortés-Gonzalez, Vianney V; Zamora-Ortiz, Rocio R; Kohl, Susanne S; Kuehlewein, Laura L; Darvish, Hossein H; Alehabib, Elham E; Arenas-Sordo, Maria de la Luz ML; Suri, Fatemeh F; Vona, Barbara B; Haaf, Thomas T
Publication Date: 2022-04

Variant appearance in text: USH2A: 11357del
PubMed Link: 34148116
Variant Present in the following documents:
  • Main text
  • 439_2021_Article_2303.pdf
  • 439_2021_2303_MOESM1_ESM.pdf
View BVdb publication page