The Contribution of Mosaic Variants to Autism Spectrum Disorder

PLoS Genetics

Volumn 12, Issue 9, 2016, Pages

  Freed, Donald ^a,b   Pevsner, Jonathan ^a,b  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b KENNEDY KRIEGER INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MYOSIN HEAVY CHAIN; NCK PROTEIN; DNA BINDING PROTEIN; MLL2 PROTEIN, HUMAN; MYOSIN IIB; NCKAP1 PROTEIN, HUMAN; NONMUSCLE MYOSIN TYPE IIB HEAVY CHAIN; SIGNAL TRANSDUCING ADAPTOR PROTEIN; TUMOR PROTEIN;

ARTICLE; ASCERTAINMENT BIAS; AUTISM; CHILD; CLINICAL ARTICLE; CONCEPTION; CONTROLLED STUDY; EXOME; GENE DISRUPTION; GENE MUTATION; GENE SEQUENCE; GENETIC MODEL; GENETIC RISK; GENETIC VARIABILITY; GENETIC VARIATION; GERM CELL; HERITABILITY; HUMAN; HUMAN TISSUE; KMT2C GENE; MISSENSE MUTATION; MONOZYGOTIC TWINS; MOSAICISM; MUTATION RATE; MUTATIONAL ANALYSIS; MUTATOR GENE; MYH10 GENE; NCKAP1 GENE; SIBLING; TISSUE SPECIFICITY; TWIN DISCORDANCE; ADOLESCENT; ADULT; ANTIBODY SPECIFICITY; FEMALE; GENETIC PREDISPOSITION; GENETICS; MALE; MIDDLE AGED; PATHOLOGY; PRESCHOOL CHILD;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; ADOLESCENT; ADULT; AUTISM SPECTRUM DISORDER; CHILD; CHILD, PRESCHOOL; DNA-BINDING PROTEINS; EXOME; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MIDDLE AGED; MOSAICISM; MUTATION, MISSENSE; MYOSIN HEAVY CHAINS; NEOPLASM PROTEINS; NONMUSCLE MYOSIN TYPE IIB; ORGAN SPECIFICITY; SIBLINGS;

EID: 84990231487     PISSN: 15537390     EISSN: 15537404     Source Type: Journal    
DOI: 10.1371/journal.pgen.1006245     Document Type: Article

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