Meis1 p.r272h in familial restless legs syndrome

Neurology

Volumn 73, Issue 3, 2009, Pages 243-245

  Vilarino Guell C ^a,e   Chai, H ^a   Keeling, B H ^a   Young, J E ^a   Rajput, A ^a,b   Lynch, T ^c   Aaslv, J O ^d   Uitti, R J ^a   Wszolek, Z K ^a   Farrer, M J ^a   Lin, S C ^a  

^a MAYO GRADUATE SCHOOL   (United States)

^b UNIVERSITY OF SASKATCHEWAN   (Canada)

^c MATER MISERICORDIAE UNIVERSITY HOSPITAL   (Ireland)

^d NORWEGIAN UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Norway)

^e MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA; BTBD9 PROTEIN, HUMAN; HOMEODOMAIN PROTEIN; MYELOID ECOTROPIC VIRAL INTEGRATION SITE 1 PROTEIN; TRANSCRIPTION FACTOR; TUMOR PROTEIN;

ADOLESCENT; ADULT; AGED; ARTICLE; BTBD9 GENE; CHILD; CONTROLLED STUDY; DNA DETERMINATION; FAMILIAL DISEASE; FAMILY; GENE DELETION; GENE SEQUENCE; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; HUMAN; MAJOR CLINICAL STUDY; MEIS1 GENE; MUTATION; NONHUMAN; NUCLEOTIDE SEQUENCE; PEDIGREE; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; PRIORITY JOURNAL; RESTLESS LEGS SYNDROME; SCHOOL CHILD; SEQUENCE ANALYSIS; CASE CONTROL STUDY; FAMILY HEALTH; FEMALE; GENETIC MARKER; GENETIC PREDISPOSITION; GENETIC SCREENING; GENETICS; GENOTYPE; INHERITANCE; MALE; MIDDLE AGED; MOLECULAR GENETICS; PATHOPHYSIOLOGY; PREVALENCE; PROTEIN TERTIARY STRUCTURE;

AGED; BASE SEQUENCE; CASE-CONTROL STUDIES; CONSERVED SEQUENCE; DNA MUTATIONAL ANALYSIS; FAMILY HEALTH; FEMALE; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; GENETIC SCREENING; GENOTYPE; HOMEODOMAIN PROTEINS; HUMANS; INHERITANCE PATTERNS; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MUTATION; NEOPLASM PROTEINS; PEDIGREE; PREVALENCE; PROTEIN STRUCTURE, TERTIARY; RESTLESS LEGS SYNDROME; TRANSCRIPTION FACTORS;

EID: 68949194365     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/WNL.0b013e3181ae7c79     Document Type: Article

References (7)

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