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Gene Mutations in Apical Hypertrophic Cardiomyopathy
Author(s) -
Michael Arad,
Manual Penas-Lado,
Lorenzo Monserrat,
Barry J. Maron,
Mark V. Sherrid,
Carolyn Y. Ho,
Scott Barr,
Ahmad Karim,
Timothy M. Olson,
Mitsohiro Kamisago,
Jonathan G. Seidman,
Christine E. Seidman
Publication year - 2005
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.105.547448
Subject(s) - hypertrophic cardiomyopathy , missense mutation , proband , sarcomere , muscle hypertrophy , gene mutation , genetics , mutation , medicine , gene , biology , myocyte
Nonobstructive hypertrophy localized to the cardiac apex is an uncommon morphological variant of hypertrophic cardiomyopathy (HCM) that often is further distinguished by distinct giant negative T waves and a benign clinical course. The genetic relationship between HCM with typical hypertrophic morphology versus isolated apical hypertrophy is incompletely understood.

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