Movement disorder and neuronal migration disorder due to ARFGEF2 mutation

Neurogenetics

Volumn 10, Issue 4, 2009, Pages 333-336

  De Wit, M C Y ^a   De Coo, I F M ^a   Halley, D J J ^a   Lequin, M H ^a   Mancini, G M S ^a  

^a SOPHIA CHILDREN S HOSPITAL   (Netherlands)

Author keywords

ARFGEF2; Basal ganglia; BIG2; Bilateral periventricular nodular heterotopia; Child; Extrapyramidal movement disorder; FLNA; Microcephaly

Indexed keywords

ARFGEF2 PROTEIN, HUMAN; GUANINE NUCLEOTIDE EXCHANGE FACTOR;

ARTICLE; BRAIN; CELL MOTION; CHILD; CYTOLOGY; FEMALE; GENETICS; HUMAN; MALE; MICROCEPHALY; MOLECULAR GENETICS; MOTOR DYSFUNCTION; MULTIPLE MALFORMATION SYNDROME; MUTATION; NERVE CELL; NUCLEOTIDE SEQUENCE; PATHOLOGY; PATHOPHYSIOLOGY; PERIVENTRICULAR HETEROTOPIA; PHENOTYPE; PHYSIOLOGY;

ABNORMALITIES, MULTIPLE; BASE SEQUENCE; BRAIN; CELL MOVEMENT; CHILD; DNA MUTATIONAL ANALYSIS; FEMALE; GUANINE NUCLEOTIDE EXCHANGE FACTORS; HUMANS; MALE; MICROCEPHALY; MOLECULAR SEQUENCE DATA; MOVEMENT DISORDERS; MUTATION; NEURONS; PERIVENTRICULAR NODULAR HETEROTOPIA; PHENOTYPE;

EID: 79953675536     PISSN: 13646745     EISSN: 13646753     Source Type: Journal    
DOI: 10.1007/s10048-009-0192-2     Document Type: Article

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