Clinical utility gene card for: hypertrophic cardiomyopathy (type 1–14)

@article{Pinto2011ClinicalUG,
  title={Clinical utility gene card for: hypertrophic cardiomyopathy (type 1–14)},
  author={Y. Pinto and A. Wilde and I. A. V. Rijsingen and I. Christiaans and R. H. L. Deprez and P. Elliott},
  journal={European Journal of Human Genetics},
  year={2011},
  volume={19},
  pages={-}
}
1.2 OMIM# of the disease 192600 Cardiomyopathy, familial hypertrophic; CMH. 115195 Cardiomyopathy, familial hypertrophic, 2; CMH2. 115196 Cardiomyopathy, familial hypertrophic, 3; CMH3. 115197 Cardiomyopathy, familial hypertrophic, 4; CMH4. 600858 Cardiomyopathy, familial hypertrophic, 6; CMH6. +191044 Cardiomyopathy, familial hypertrophic, 7; CMH7. 608751 Cardiomyopathy, familial hypertrophic, 8; CMH8. +191044 Cardiomyopathy, familial hypertrophic, 9; CMH9. 608758 Cardiomyopathy, familial… Expand
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Background Citations
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19 Citations

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Citation Type

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Pregnancy, cardiomyopathies, and genetics.
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Next-generation sequencing (NGS) as a molecular diagnostic tool for hypertrophic cardiomyopathy in a Chinese boy due to novel compound heterozygous mutations in the MYBPC3 gene
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Cardiomyopathies
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Genetic testing for predisposition to inherited hypertrophic cardiomyopathy.
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