Mutations in IFT172 cause isolated retinal degeneration and Bardet–Biedl syndromeKinga M. Bujakowska, Eric A. Pierce, Emily Place et al.|Human Molecular Genetics|2014Cited by 160
<scp> <i>WDR34</i> </scp> , a candidate gene for non‐syndromic rod‐cone dystrophyMaria Solaguren‐Beascoa, Christina Zeitz, Kinga M. Bujakowska et al.|Clinical Genetics|2020Cited by 12