Eye tracking dysfunction is a putative phenotypic susceptibility marker of schizophrenia and maps to a locus on chromosome 6p in families with multiple occurrence of the disease

American Journal of Medical Genetics - Seminars in Medical Genetics

Volumn 67, Issue 6, 1996, Pages 564-579

  Arolt, Volker ^a   Lencer, Rebekka ^a   Nolte, Achim ^a   Müller Myhsok, Bertram ^b   Purmann, Sabine ^a   Schürmann, Manfred ^a   Leutelt, Jutta ^a   Pinnow, Marlene ^a   Schwinger, Eberhard ^a  

^a UNIVERSITY OF LÜBECK   (Germany)

^b BERNHARD NOCHT INSTITUTE FOR TROPICAL MEDICINE   (Germany)

Author keywords

Biological markers; Eye movements; Eye tracking dysfunction; Linkage; Schizophrenia

Indexed keywords

BIOLOGICAL MARKER;

ARTICLE; CHROMOSOME 6P; CLINICAL ARTICLE; EYE MOVEMENT; EYE MOVEMENT DISORDER; EYE TRACKING; FAMILY STUDY; GENE MAPPING; GENETIC LINKAGE; GENETIC MODEL; GENETIC SUSCEPTIBILITY; HUMAN; PEDIGREE ANALYSIS; PHENOTYPE; PRIORITY JOURNAL; PSYCHOSIS; SCHIZOPHRENIA;

ADULT; AGED; BIOLOGICAL MARKERS; CHROMOSOMES, HUMAN, PAIR 6; HUMANS; INFRARED RAYS; LINKAGE (GENETICS); MIDDLE AGED; OCULAR MOTILITY DISORDERS; PEDIGREE; SCHIZOPHRENIA;

EID: 0029819112     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19961122)67:6<564::AID-AJMG10>3.0.CO;2-R     Document Type: Article

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