TY  - GEN
AU  - van Bon,B W M
AU  - Coe,B P
AU  - Bernier,R
AU  - Green,C
AU  - Gerdts,J
AU  - Witherspoon,K
AU  - Kleefstra,T
AU  - Willemsen,M H
AU  - Kumar,R
AU  - Bosco,P
AU  - Fichera,M
AU  - Li,D
AU  - Amaral,D
AU  - Cristofoli,F
AU  - Peeters,H
AU  - Haan,E
AU  - Romano,C
AU  - Mefford,H C
AU  - Scheffer,I
AU  - Gecz,J
AU  - de Vries,B B A
AU  - Eichler,E E
TI  - Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID
SN  - 1476-5578
PY  - 2016///0916
KW  - Adolescent
KW  - Adult
KW  - Autistic Disorder
KW  - genetics
KW  - Child
KW  - Child, Preschool
KW  - Cohort Studies
KW  - Female
KW  - Fetal Growth Retardation
KW  - Humans
KW  - Intellectual Disability
KW  - Male
KW  - Microcephaly
KW  - Middle Aged
KW  - Mutation
KW  - Phenotype
KW  - Protein Serine-Threonine Kinases
KW  - Protein-Tyrosine Kinases
KW  - Seizures, Febrile
KW  - Siblings
KW  - Speech Disorders
KW  - Stereotypic Movement Disorder
KW  - Syndrome
KW  - Young Adult
KW  - Dyrk Kinases
N1  - Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1038/mp.2015.5
ER  -