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De novo variants in SUPT16H cause neurodevelopmental disord..:
Bina, Roya
;
Matalon, Dena
;
Fregeau, Brieana
...
qt42t3t7jh. , 2020
Link:
https://escholarship.org/uc/item/42t3t7jh
RT Journal T1
De novo variants in SUPT16H cause neurodevelopmental disorders associated with corpus callosum abnormalities
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt42t3t7jh&Exemplar=1&LAN=DE A1 Bina, Roya A1 Matalon, Dena A1 Fregeau, Brieana A1 Tarsitano, Jacqueline Joani A1 Aukrust, Ingvild A1 Houge, Gunnar A1 Bend, Renee A1 Warren, Hannah A1 Stevenson, Roger E A1 Stuurman, Kyra Eva A1 Barkovich, A James A1 Sherr, Elliott H PB eScholarship, University of California YR 2020 K1 Biological Sciences K1 Bioinformatics and Computational Biology K1 Biomedical and Clinical Sciences K1 Genetics K1 Clinical Sciences K1 Human Genome K1 Brain Disorders K1 Neurosciences K1 Intellectual and Developmental Disabilities (IDD) K1 Clinical Research K1 2.1 Biological and endogenous factors K1 Aetiology K1 Adolescent K1 Agenesis of Corpus Callosum K1 Brain K1 Cell Cycle Proteins K1 Child K1 Preschool K1 Corpus Callosum K1 Exome K1 Female K1 Genetic Predisposition to Disease K1 Humans K1 Intellectual Disability K1 Male K1 Mutation K1 Missense K1 Neurodevelopmental Disorders K1 Seizures K1 Transcription Factors K1 Exome Sequencing K1 developmental K1 other neurology K1 Medical and Health Sciences K1 Genetics & Heredity JF qt42t3t7jh LK http://dx.doi.org/https://escholarship.org/uc/item/42t3t7jh DO https://escholarship.org/uc/item/42t3t7jh SF ELIB - SuUB Bremen
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