Gillentine, Madelyn A ;
Wang, Tianyun ;
Hoekzema, Kendra...
Gillentine , M A , Wang , T , Hoekzema , K , Rosenfeld , J , Liu , P , Guo , H , Kim , C N , De Vries , B B A , Vissers , L E L M , Nordenskjold , M , Kvarnung , M , Lindstrand , A , Nordgren , A , Gecz , J , Iascone , M , Cereda , A , Scatigno , A , Maitz , S , Zanni , G , Bertini , E , Zweier , C , Schuhmann , S , Wiesener , A , Pepper , M , Panjwani , H , Torti , E , Abid , F , Anselm , I , Srivastava , S , Atwal , P , Bacino , C A , Bhat , G , Cobian , K , Bird , L M , Friedman , J , Wright , M S , Callewaert , B , Petit , F , Mathieu , S , Afenjar , A , Christensen , C K , White , K M , Elpeleg , O , Berger , I , Espineli , E J , Fagerberg , C , Brasch-Andersen , C , Hansen , L K , Lauridsen , M , Sorensen , K , CAUSES Study & SPARK Consortium 2021 , ' Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders ' , Genome Medicine , vol. 13 , pp. 63 . https://doi.org/10.1186/s13073-021-00870-6.
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2021
