LIPC c.574+467C>T

Variant ID: 15-58835317-C-T

NM_000236.2(LIPC):c.574+467C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Novel C8orf37 mutations cause retinitis pigmentosa in consanguineous families of Pakistani origin.

Molecular Vision
Ravesh, Zeinab Z; El Asrag, Mohammed E ME; Weisschuh, Nicole N; McKibbin, Martin M; Reuter, Peggy P; Watson, Christopher M CM; Baumann, Britta B; Poulter, James A JA; Sajid, Sundus S; Panagiotou, Evangelia S ES; O'Sullivan, James J; Abdelhamed, Zakia Z; Bonin, Michael M; Soltanifar, Mehdi M; Black, Graeme C M GC; Amin-ud Din, Muhammad M; Toomes, Carmel C; Ansar, Muhammad M; Inglehearn, Chris F CF; Wissinger, Bernd B; Ali, Manir M
Publication Date: 2015

Variant appearance in text: rs16940472
PubMed Link: 25802487
Variant Present in the following documents:
  • Main text
  • mv-v21-236.pdf
View BVdb publication page