BBS2 c.117+1G>T

Variant ID: 16-56553657-C-A

NM_031885.3(BBS2):c.117+1G>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Targeted next generation sequencing reveals genetic defects underlying inherited retinal disease in Iranian families.

Molecular Vision
Tayebi, Naeimeh N; Akinrinade, Oyediran O; Khan, Muhammad Imran MI; Hejazifar, Arash A; Dehghani, Alireza A; Cremers, Frans P M FPM; Akhlaghi, Mohammadreza M
Publication Date: 2019

Variant appearance in text: BBS2: 117+1G>T
PubMed Link: 30820146
Variant Present in the following documents:
  • Main text
  • mv-v25-106.pdf
View BVdb publication page