Mutational spectrum in the Ca 2+-activated cation channel gene TRPM4 in patients with cardiac conductance disturbances

Human Mutation

Volumn 33, Issue 1, 2012, Pages 109-117

  Stallmeyer, Birgit ^a,b   Zumhagen, Sven ^a   Denjoy, Isabelle ^c,d   Duthoit, Guillaume ^c   Hébert, Jean Louis ^e   Ferrer, Xavier ^f   Maugenre, Svetlana ^c,g   Schmitz, Wilhelm ^a   Kirchhefer, Uwe ^a   Schulze Bahr, Ellen ^a   Guicheney, Pascale ^c,g   Schulze Bahr, Eric ^a,b  

^a UNIVERSITY HOSPITAL MÜNSTER   (Germany)

^b UNIVERSITY OF MÜNSTER   (Germany)

^c PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^d HÔPITAL LARIBOISIÈRE   (France)

^e BICÊTRE HOSPITAL   (France)

^f BORDEAUX UNIVERSITY HOSPITAL   (France)

^g SORBONNE UNIVERSITÉ   (France)

Author keywords

Atrioventricular block; Cardiac conduction disease; Rightbundle branch block; TRPM4

Indexed keywords

TRANSIENT RECEPTOR POTENTIAL CHANNEL M4;

ADOLESCENT; ADULT; AMINO ACID SUBSTITUTION; ARTICLE; ATRIOVENTRICULAR BLOCK; BRUGADA SYNDROME; CHILD; CONTROLLED STUDY; CYTOPLASM; FEMALE; GAIN OF FUNCTION MUTATION; GENE DELETION; GENETIC ASSOCIATION; GENETIC VARIABILITY; HEART ARRHYTHMIA; HEART RIGHT BUNDLE BRANCH BLOCK; HETEROZYGOSITY; HUMAN; INFANT; LONG QT SYNDROME; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; PROTEIN LOCALIZATION; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; SINUS NODE DYSFUNCTION;

ADOLESCENT; ADULT; AMINO ACID SEQUENCE; ATRIOVENTRICULAR BLOCK; BUNDLE-BRANCH BLOCK; CALCIUM; CASE-CONTROL STUDIES; COHORT STUDIES; DNA MUTATIONAL ANALYSIS; ELECTROCARDIOGRAPHY; FEMALE; GENOTYPE; HEART; HUMANS; INFANT; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE; PHENOTYPE; POLYMORPHISM, GENETIC; SEQUENCE DELETION; TRPM CATION CHANNELS;

EID: 84857687674     PISSN: 10597794     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.21599     Document Type: Article

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