McLeod syndrome: Life-long neuropsychiatric disorder due to a novel mutation of the XK gene

Psychiatric Genetics

Volumn 15, Issue 4, 2005, Pages 291-293

  Zeman, Adam ^a   Daniels, Geoff ^b   Tilley, Louise ^b   Dunn, Margaret ^c   Toplis, Laura ^c   Bullock, Tom ^b   Poole, Joyce ^b   Blackwood, Douglas ^c  

^a UNIVERSITY OF EDINBURGH   (United Kingdom)

^b NHS BLOOD AND TRANSPLANT   (United Kingdom)

^c ROYAL EDINBURGH HOSPITAL   (United Kingdom)

Author keywords

Acanthocytosis; Basal ganglia; Chorea; McLeod syndrome; Neuropsychiatry; XK gene

Indexed keywords

CREATINE KINASE;

ACANTHOCYTOSIS; ADULT; AREFLEXIA; ARTICLE; BEHAVIOR CHANGE; BLOOD; CASE REPORT; CHOREA; CLINICAL ASSESSMENT; DYSARTHRIA; EXON; GENE; GENE MUTATION; HUMAN; IMPULSIVENESS; MALE; NEUROACANTHOCYTOSIS; NEUROPSYCHIATRY; NEUROPSYCHOLOGY; PERFUSION; PHENOTYPE; PRIORITY JOURNAL; PSYCHOPATHY; STOP CODON; XK GENE; CENTRAL NERVOUS SYSTEM DISEASE; CHROMOSOME DISORDER; GENETICS; MIDDLE AGED; MUTATION; NEUROLOGIC DISEASE; PATHOLOGY; SYNDROME; X CHROMOSOME;

ACANTHOCYTES; CENTRAL NERVOUS SYSTEM DISEASES; CHROMOSOMES, HUMAN, X; HUMANS; MALE; MIDDLE AGED; MUTATION; NERVOUS SYSTEM DISEASES; SEX CHROMOSOME DISORDERS; SYNDROME;

EID: 33645733916     PISSN: 09558829     EISSN: None     Source Type: Journal    
DOI: 10.1097/00041444-200512000-00012     Document Type: Article

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