Myofibrillar myopathy with arrhythmogenic right ventricular cardiomyopathy 7: Corroboration and narrowing of the critical region on 10q22.3

European Journal of Human Genetics

Volumn 16, Issue 3, 2008, Pages 367-373

  Kuhl, Angelika ^a   Melberg, Atle ^b   Meinl, Edgar ^a,c   Nürnberg, Gudrun ^d   Nürnberg, Peter ^d   Kehrer Sawatzki, Hildegard ^e   Jenne, Dieter E ^a  

^a MAX PLANCK INSTITUTE OF NEUROBIOLOGY   (Germany)

^b UPPSALA UNIVERSITY HOSPITAL   (Sweden)

^c UNIVERSITY OF MUNICH   (Germany)

^d UNIVERSITY OF COLOGNE   (Germany)

^e UNIVERSITY OF ULM   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY PROTEIN 7; CHROMOSOME PROTEIN; GENE PRODUCT; METAVINCULIN; PROTEIN ANXA11; PROTEIN C10ORF56; PROTEIN C10ORF57; PROTEIN C10ORF58; PROTEIN DYDC1; PROTEIN DYDC2; PROTEIN MAT1A; PROTEIN PLAC9; PROTEIN PPIF; PROTEIN RAI17; PROTEIN SFTPA1; PROTEIN SFTPA1B; PROTEIN SFTPA2; PROTEIN SFTPA2B; PROTEIN SFTPD; PROTEIN SH2D4B; PROTEIN TSPAN14; PROTEIN ZASP; UNCLASSIFIED DRUG;

ALLELE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 10P; CHROMOSOME MAP; CONGESTIVE CARDIOMYOPATHY; EXON; FEMALE; GENE DELETION; GENE IDENTIFICATION; GENE LOCUS; GENETIC CODE; GENETIC LINKAGE; HEART RIGHT VENTRICLE DYSPLASIA; HUMAN; HUMAN CELL; HUMAN TISSUE; HYBRID CELL; MALE; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROMOTER REGION; SEQUENCE TAGGED SITE; SINGLE NUCLEOTIDE POLYMORPHISM;

ARRHYTHMIAS, CARDIAC; CHROMOSOMES, HUMAN, PAIR 10; DNA PRIMERS; FEMALE; GENOTYPE; HUMANS; HYPERTROPHY, RIGHT VENTRICULAR; LINKAGE (GENETICS); MALE; MUTATION; PEDIGREE;

EID: 39749125673     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5201980     Document Type: Article

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