Heterozygous variants in CTR9, which encodes a major component of the PAF1 complex, are associated with a neurodevelopmental disorder

Authors :: Meuwissen, Marije
Verstraeten, Aline
Ranza, E.
Iwaszkiewicz, Justyna
Bastiaansen, Maaike
Mateiu, Ligia
Vulto-van Silfhout, A.T.
Kleefstra, T.
Antonarakis, Stylianos E.
Loeys, B.L.
Meuwissen, Marije
Verstraeten, Aline
Ranza, E.
Iwaszkiewicz, Justyna
Bastiaansen, Maaike
Mateiu, Ligia
Vulto-van Silfhout, A.T.
Kleefstra, T.
Antonarakis, Stylianos E.
Loeys, B.L.
Source :: Genetics in Medicine; 1583; 1591; 1098-3600; 7; 24; ~Genetics in Medicine~1583~1591~~~1098-3600~7~24~~
Publication Year :: 2022
Abstract: Item does not contain fulltext

Database :: OAIster
Journal :: Genetics in Medicine; 1583; 1591; 1098-3600; 7; 24; ~Genetics in Medicine~1583~1591~~~1098-3600~7~24~~
Publication Type :: Electronic Resource
Accession number :: edsoai.on1367213882
Document Type :: Electronic Resource

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