PROK2 c.96+4A>G

Variant ID: 3-71834104-T-C

NM_001126128.1(PROK2):c.96+4A>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Novel Genomic Variants, Atypical Phenotypes and Evidence of a Digenic/Oligogenic Contribution to Disorders/Differences of Sex Development in a Large North African Cohort.

Frontiers In Genetics
Zidoune, Housna H; Ladjouze, Asmahane A; Chellat-Rezgoune, Djalila D; Boukri, Asma A; Dib, Scheher Aman SA; Nouri, Nassim N; Tebibel, Meryem M; Sifi, Karima K; Abadi, Noureddine N; Satta, Dalila D; Benelmadani, Yasmina Y; Bignon-Topalovic, Joelle J; El-Zaiat-Munsch, Maeva M; Bashamboo, Anu A; McElreavey, Ken K
Publication Date: 2022

Variant appearance in text: PROK2: 96+4A>G
PubMed Link: 36110220
Variant Present in the following documents:
  • Main text
  • fgene-13-900574.pdf
View BVdb publication page