BBS7 c.785_786del ;(p.D262Gfs*8)

Variant ID: 4-122774174-CAT-C

NM_176824.2(BBS7):c.785_786del;(p.D262Gfs*8)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Nationwide genetic analysis of more than 600 families with inherited eye diseases in Argentina.

Npj Genomic Medicine
Schlottmann, Patricio G PG; Luna, José D JD; Labat, Natalia N; Yadarola, María Belén MB; Bainttein, Silvina S; Esposito, Evangelina E; Ibañez, Agustina A; Barbaro, Evangelina Ivón EI; Álvarez Mendiara, Alejandro A; Picotti, Carolina P CP; Chirino Misisian, Andrea A; Andreussi, Luciana L; Gras, Julieta J; Capalbo, Luciana L; Visotto, Mauro M; Dipierri, José E JE; Alcoba, Emilio E; Fernández Gabrielli, Laura L; Ávila, Silvia S; Aucar, María Emilia ME; Martin, Daniel M DM; Ormaechea, Gerardo Juan GJ; Inga, M Eugenia ME; Francone, Aníbal A AA; Charles, Martin M; Zompa, Tamara T; Pérez, Pablo Javier PJ; Lotersztein, Vanesa V; Nuova, Pedro J PJ; Canonero, Ivana B IB; Mahroo, Omar A OA; Michaelides, Michel M; Arno, Gavin G; Daich Varela, Malena M
Publication Date: 2023-05-22

Variant appearance in text: BBS7: 785_786del; Asp262Glyfs*8
PubMed Link: 37217489
Variant Present in the following documents:
  • 41525_2023_Article_352.pdf
  • 41525_2023_352_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page