Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID. [electronic resource]
Producer: 20160916Description: 126-32 p. digitalISSN:- 1476-5578
- Adolescent
- Adult
- Autistic Disorder -- genetics
- Child
- Child, Preschool
- Cohort Studies
- Female
- Fetal Growth Retardation -- genetics
- Humans
- Intellectual Disability -- genetics
- Male
- Microcephaly -- genetics
- Middle Aged
- Mutation
- Phenotype
- Protein Serine-Threonine Kinases -- genetics
- Protein-Tyrosine Kinases -- genetics
- Seizures, Febrile -- genetics
- Siblings
- Speech Disorders -- genetics
- Stereotypic Movement Disorder -- genetics
- Syndrome
- Young Adult
- Dyrk Kinases
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Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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