Taylor, Rachel L ;
Soriano, Carla Sanjuro ;
Williams, Simon...
Taylor , R L , Soriano , C S , Williams , S , Dzulova , D , Ashworth , J , Hall , G , Gale , T , Lloyd , I C , Inglehearn , C F , Toomes , C , Douzgou , S & Black , G 2022 , ' Bi-allelic mutation of CTNNB1 causes a severe form of syndromic microphthalmia, persistent foetal vasculature and vitreoretinal dysplasia ' , Orphanet Journal of Rare Diseases , vol. 17 , 110 . https://doi.org/10.1186/s13023-022-02239-3.
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2022