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Heterozygous variants in CTR9, which encodes a major compon..:
Meuwissen, Marije
;
Verstraeten, Aline
;
Ranza, Emmanuelle
...
Genetics in Medicine. 24 (2022) 7 - p. 1583-1591 , 2022
Link:
https://doi.org/10.1016/j.gim.2022.04.003
RT Journal T1
Heterozygous variants in CTR9, which encodes a major component of the PAF1 complex, are associated with a neurodevelopmental disorder
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.gim.2022.04.003&Exemplar=1&LAN=DE A1 Meuwissen, Marije A1 Verstraeten, Aline A1 Ranza, Emmanuelle A1 Iwaszkiewicz, Justyna A1 Bastiaansen, Maaike A1 Mateiu, Ligia A1 Nemegeer, Merlijn A1 Meester, Josephina A.N. A1 Afenjar, Alexandra A1 Amaral, Michelle A1 Ballhausen, Diana A1 Barnett, Sarah A1 Barth, Magalie A1 Asselbergh, Bob A1 Spaas, Katrien A1 Heeman, Bavo A1 Bassetti, Jennifer A1 Blackburn, Patrick A1 Schaer, Marie A1 Blanc, Xavier A1 Zoete, Vincent A1 Casas, Kari A1 Courtin, Thomas A1 Doummar, Diane A1 Guerry, Frédéric A1 Keren, Boris A1 Pappas, John A1 Rabin, Rachel A1 Begtrup, Amber A1 Shinawi, Marwan PB Elsevier BV YR 2022 SN 1098-3600 JF Genetics in Medicine VO 24 IS 7 SP 1583 OP 1591 LK http://dx.doi.org/https://doi.org/10.1016/j.gim.2022.04.003 DO https://doi.org/10.1016/j.gim.2022.04.003 SF ELIB - SuUB Bremen
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