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Washington, DC: American Association for Clinical Chemistry
Erscheinungsjahr
2011
Link zum Volltext
Quelle
Oxford Journals 2020 Medicine
Beschreibungen/Notizen
Two of the patients were familial HCM patients who were carriers of missense mutations in the MYH72 (myosin, heavy chain 7, cardiac muscle, beta) gene (Val822Met and Arg453Cys). Author Contributions: All authors confirmed they have contributed to the intellectual content of this paper and have met the following 3 requirements: (a) significant contributions to the conception and design, acquisition of data, or analysis and interpretation of data; (b) drafting or revising the article for intellectual content; and (c) final approval of the published article.