Cellular and molecular aspects of familial hypertrophic cardiomyopathy caused by mutations in the cardiac troponin I gene
2004 ◽
Vol 263
(1/2)
◽
pp. 99-114
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2001 ◽
Vol 33
(12)
◽
pp. 2095-2107
◽
2011 ◽
Vol 97
(1)
◽
pp. 155-169
◽
2006 ◽
Vol 41
(4)
◽
pp. 623-632
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Keyword(s):
Keyword(s):
Keyword(s):
2000 ◽
Vol 32
(3)
◽
pp. 521-525
◽
Keyword(s):
Keyword(s):