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PubPharm (177)
171
839-3 Frequency, spectrum, and phenotype of hypertrophic cardiomyopathy patients with multiple sarcomeric mutations
enthalten in:
Journal of the American College of Cardiology
| 2004
von
Van Driest, S.
|
Ommen, S.
|
Will, M.
| +5
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172
Comprehensive analysis of the beta-myosin heavy chain gene in 389 unrelated patients with hypertrophic cardiomyopathy
enthalten in:
Journal of the American College of Cardiology
| 2004
von
Van Driest, S.
|
Jaeger, M.
|
Ommen, S.
| +4
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173
Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy
enthalten in:
Circulation
| 2003
von
Van Driest, S.
|
Ellsworth, E.
|
Ommen, S.
| +3
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174
Prevalence and severity of "benign" mutations in the beta-myosin heavy chain, cardiac troponin T, and alpha-tropomyosin genes in hypertrophic cardiomyopathy
enthalten in:
Circulation
| 2002
von
Van Driest, S.
|
Ackerman, M.
|
Ommen, S.
| +5
CommentIn: Circulation. 2003 Jul 29;108(4):e24-5; author reply e24-5. - PMID 12885737
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175
A novel TPM1 mutation in a family with hypertrophic cardiomyopathy and sudden cardiac death in childhood
enthalten in:
The American journal of cardiology
| 2002
von
Van Driest, S.
|
Will, M.
|
Atkins, D.
| +1
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176
Prevalence and age-dependence of malignant mutations in the beta-myosin heavy chain and troponin T genes in hypertrophic cardiomyopathy : a comprehensive outpatient perspective
enthalten in:
Journal of the American College of Cardiology
| 2002
von
Ackerman, M.
|
VanDriest, S.
|
Ommen, S.
| +4
CommentIn: J Am Coll Cardiol. 2002 Jun 19;39(12):2049-51. - PMID 12084607
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177
A novel TPM1 mutation in a family with hypertrophic cardiomyopathy and sudden cardiac death in childhood
enthalten in:
The American journal of cardiology
| 2002
von
Van Driest, S.
|
Will, M.
|
Atkins, D.
| +1
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69
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21
EC 1.14.14.1
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Cytochrome P-450 CYP2D6
10
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9
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9
pharmacogenetics
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pharmacogenomics
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pediatrics
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Creatinine
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CYP2C19 protein, human
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