Published in
Elsevier, Genetics in Medicine, 7(24), p. 1583-1591, 2022
DOI: 10.1016/j.gim.2022.04.003
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Heterozygous variants in CTR9, which encodes a major component of the PAF1 complex, are associated with a neurodevelopmental disorder
Journal article published in 2022 by
Marije Meuwissen 
,
Aline Verstraeten,
Emmanuelle Ranza,
Justyna Iwaszkiewicz,
Maaike Bastiaansen,
Ligia Mateiu,
Merlijn Nemegeer,
Josephina A. N. Meester,
Alexandra Afenjar,
Michelle Amaral,
Diana Ballhausen,
Sarah Barnett,
Magalie Barth,
Bob Asselbergh,
Katrien Spaas
and other authors.
,
Aline Verstraeten,
Emmanuelle Ranza,
Justyna Iwaszkiewicz,
Maaike Bastiaansen,
Ligia Mateiu,
Merlijn Nemegeer,
Josephina A. N. Meester,
Alexandra Afenjar,
Michelle Amaral,
Diana Ballhausen,
Sarah Barnett,
Magalie Barth,
Bob Asselbergh,
Katrien Spaas
and other authors.
This paper was not found in any repository, but could be made available legally by the author.
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