Exome sequencing in a family with restless legs syndrome

Movement Disorders

Volumn 27, Issue 13, 2012, Pages 1686-1689

  Weissbach, Anne ^a   Siegesmund, Katharina ^a   Brüggemann, Norbert ^a   Schmidt, Alexander ^a   Kasten, Meike ^a   Pichler, Irene ^a,b   Muhle, Hiltrud ^c   Lohmann, Ebba ^d   Lohnau, Thora ^a   Schwinger, Eberhard ^a   Hagenah, Johann ^a   Stephani, Ulrich ^c   Pramstaller, Peter P ^a,b   Klein, Christine ^a   Lohmann, Katja ^a  

^a UNIVERSITY OF LÜBECK   (Germany)

^b University of Lubeck   (Italy)

^c UNIVERSITY OF KIEL   (Germany)

^d ISTANBUL UNIVERSITY   (Turkey)

Author keywords

Genome wide linkage analysis; Next generation sequencing; PCDHA3; Restless legs syndrome

Indexed keywords

ADULT; ARTICLE; ATRN GENE; CONTROLLED STUDY; EXOME; EXON; FAMILIAL DISEASE; FAT2 GENE; FEMALE; GENE; GENE FREQUENCY; GENE LOCUS; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC RISK; GENETIC VARIABILITY; GERMANY; HUMAN; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PCDHA3 GENE; PRIORITY JOURNAL; RESTLESS LEGS SYNDROME; WWC2 GENE;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; CADHERINS; DNA MUTATIONAL ANALYSIS; EXOME; FAMILY HEALTH; FEMALE; GENETIC ASSOCIATION STUDIES; GENETIC LINKAGE; GERMANY; HUMANS; MALE; MEMBRANE PROTEINS; RESTLESS LEGS SYNDROME; RISK FACTORS;

EID: 84870336681     PISSN: 08853185     EISSN: 15318257     Source Type: Journal    
DOI: 10.1002/mds.25191     Document Type: Article

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