← Evidence map

ArticleHuman genetics2012

An Alu repeat-mediated genomic GCNT2 deletion underlies congenital cataracts and adult i blood group.

Guntram Borck et al.PubMed ↗Publisher ↗

No numbers read from the abstract.

10 papers cite it

2012
2013
2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 21761136