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Article

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

European journal of human genetics : EJHG - 1 Mar 2008

Kuhl Angelika, Melberg Atle, Meinl Edgar, Nürnberg Gudrun, Nürnberg Peter, Kehrer-Sawatzki Hildegard, Jenne Dieter E

Abstract excerpt

Several years ago, autosomal dominant myofibrillar myopathy (MFM) in combination with arrhythmogenic right ventricular cardiomyopathy (ARVC7) was tentatively mapped to a 10.6-Mbp (million base pairs) region on chromosome 10q22.3 between D10S605 (78.9 Mbp) and D10S215 (89.5 Mbp) in a Swedish family assuming that ARVC7 was allelic with cardiomyopathy, dilated 1C (CMD1C). To date, neither the genetic defect in ARVC7...

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Source

Identifiers

PMID: 18197198
DOI: 10.1038/sj.ejhg.5201980

Genes

ANXA11
DYDC1
DYDC2
LDB3
PLAC9
PPIF
SFTPA1
SFTPA2
SFTPD
TSPAN14
VCL

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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