Hereditary myopathy with early respiratory failure is caused by mutations in the titin FN3 119 domain
Author(s) -
Carola Hedberg,
Atle Melberg,
K. Dahlbom,
Anders Oldfors
Publication year - 2013
Publication title -
brain
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.142
H-Index - 336
eISSN - 1460-2156
pISSN - 0006-8950
DOI - 10.1093/brain/awt305
Subject(s) - titin , mutation , myopathy , domain (mathematical analysis) , genetics , medicine , pathology , biology , gene , sarcomere , myocyte , mathematical analysis , mathematics
Sir, Hereditary myopathy with early respiratory failure (HMERF) is a neuromuscular disease associated with aggregation of various proteins in muscle fibres and muscle degeneration (Fig. 1) and was described in detail in several families by Edstrom et al. (1990). Linkage analyses indicated that the disease locus was in the distal part of the long arm of chromosome 2 (Nicolao et al. , 1999). Titin was a candidate gene and a missense variant that segregated with the disease in …
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