Ascertainment strategies and genotype:phenotype correlations in hypertrophic cardiomyopathy.

Ascertainment strategies and genotype:phenotype correlations in hypertrophic cardiomyopathy.

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς:	Blair, E, Redwood, C, Watkins, H
Μορφή:	Journal article
Γλώσσα:	English
Έκδοση:	2003

Παρόμοια τεκμήρια

Mutations in cis can confound genotype-phenotype correlations in hypertrophic cardiomyopathy.
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Double mutations in CIS can confound genotype-phenotype correlations in hypertrophic cardiomyopathy
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Hypertrophic cardiomyopathy:a paradigm for myocardial energy depletion.
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A Genotype-phenotype Taxonomy of Hypertrophic Cardiomyopathy
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Functional analysis of hypertrophic cardiomyopathy missense mutations in the light meromyosin region of beta myosin heavy chain
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Early onset malignant hypertrophic cardiomyopathy caused by mutations in MYBPC3
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Sudden death in hypertrophic cardiomyopathy.
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Delineating the role of adenosine monophosphate (AMP)-activated protein kinase (AMP) gamma 2 subunit in hypertrophic cardiomyopathy (HCM)
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Mutations of the light meromyosin domain of the beta-myosin heavy chain rod in hypertrophic cardiomyopathy.
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Hypertrophic cardiomyopathy mutations in the gamma 2 subunit of AMP-activated kinase suggest a central role of energy compromise in disease pathogenesis
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Comparison of the functional effects of mutations in troponin T which cause dilated and hypertrophic cardiomyopathies
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Hypertrophic cardiomyopathy in Noonan Syndrome closely mimics familial hypertrophic cardiomyopathy due to sarcomeric mutations.
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Hypertrophic Cardiomyopathy: From Phenotype and Pathogenesis to Treatment
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A troponin I mutant known to cause hypertrophic cardiomyopathy shows reduced inhibition of Ca2+ independent tension
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Genetic clues to disease pathways in hypertrophic and dilated cardiomyopathies.
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Hypertrophic cardiomyopathy mutations in MYBPC3 dysregulate myosin
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