A de novo FOXP1 variant in a patient with autism, intellectual disability and severe speech and language impairment

European Journal of Human Genetics

Volumn 23, Issue 12, 2015, Pages 1702-1707

  Lozano, Reymundo ^a   Vino, Arianna ^b   Lozano, Cristina ^a   Fisher, Simon E ^b,c   Deriziotis, Pelagia ^b  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b MAX PLANCK INSTITUTE FOR PSYCHOLINGUISTICS   (Netherlands)

^c RADBOUD UNIVERSITY   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

FORKHEAD BOX PROTEIN P1; FORKHEAD TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG; FOXP1 PROTEIN, HUMAN; REPRESSOR PROTEIN;

ADOLESCENT; ARTICLE; AUTISM; CASE REPORT; CELLULAR DISTRIBUTION; CONTROLLED STUDY; EXOME; FEMALE; GENE SEQUENCE; GENETIC TRANSCRIPTION; GENETIC VARIABILITY; HUMAN; HUMAN CELL; INTELLECTUAL IMPAIRMENT; LANGUAGE DISABILITY; MUSCLE HYPOTONIA; PHENOTYPE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SPEECH DISORDER; AUTISTIC DISORDER; GENETICS; HEK293 CELL LINE; INTELLECTUAL DISABILITY; LANGUAGE DISORDERS; METABOLISM; MUTATION; PROTEIN TRANSPORT; SYNDROME;

ADOLESCENT; AUTISTIC DISORDER; FEMALE; FORKHEAD TRANSCRIPTION FACTORS; HEK293 CELLS; HUMANS; INTELLECTUAL DISABILITY; LANGUAGE DISORDERS; MUTATION; PROTEIN TRANSPORT; REPRESSOR PROTEINS; SYNDROME;

EID: 84948710248     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/ejhg.2015.66     Document Type: Article

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