Case Report: Whole Exome Sequencing Unveils an Inherited Truncating Variant in CNTN6 (p.Ser189Ter) in a Mexican Child with Autism Spectrum Disorder.
- Resource Type
- Case Study
- Source
Journal of Autism & Developmental Disorders ; Jun2020, Vol. 50 Issue 6, p2247-2251, 5p, 1 Chart, 1 Graph- Subject
Autism Language disorders Sensory disorders Diagnosis of autism Genetics of autism Alleles Electroencephalography Hearing impaired children Hydrocephalus Magnetic resonance imaging Microcephaly Genetic mutation Physical diagnosis Stereotypes Phenotypes Genetic markers Lissencephaly Genomics Sequence analysis - Language
- ISSN
- 01623257