The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders

Human Genetics

Volumn 131, Issue 11, 2012, Pages 1687-1698

  Bacon, Claire ^a   Rappold, Gudrun A ^a  

^a UNIVERSITY OF HEIDELBERG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

FORKHEAD TRANSCRIPTION FACTOR; FOXP1 PROTEIN; TRANSCRIPTION FACTOR FOXP2; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; APRAXIA; AUTISM; COGNITIVE DEFECT; COPY NUMBER VARIATION; GENE; GENE DELETION; GENE DISRUPTION; GENETIC ASSOCIATION; GENETIC VARIABILITY; HUMAN; INTELLECTUAL IMPAIRMENT; LANGUAGE DISABILITY; MISSENSE MUTATION; MOTOR DYSFUNCTION; NERVE CELL DIFFERENTIATION; NEUROPATHOLOGY; NONHUMAN; NONSENSE MUTATION; PHENOTYPE; PRIORITY JOURNAL; PROTEIN ANALYSIS; REVIEW;

COGNITION DISORDERS; FORKHEAD TRANSCRIPTION FACTORS; HUMANS; PHENOTYPE; REPRESSOR PROTEINS;

EID: 84867581362     PISSN: 03406717     EISSN: 14321203     Source Type: Journal    
DOI: 10.1007/s00439-012-1193-z     Document Type: Review

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