Pediatric patients with RASopathy-associated hypertrophic cardiomyopathy: the multifaceted consequences of PTPN11 mutations
- DOI
- 10.1186/s13023-019-1151-0
- Published
- 2019-07-05
- Container
- Orphanet Journal of Rare Diseases
- Publisher
- Springer Science and Business Media LLC
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1186/s13023-019-1151-0,
title = {Pediatric patients with RASopathy-associated hypertrophic cardiomyopathy: the multifaceted consequences of PTPN11 mutations},
author = {Giulio Calcagni and Maria Cristina Digilio and Bruno Marino and Marco Tartaglia},
year = {2019},
journal = {Orphanet Journal of Rare Diseases},
doi = {10.1186/s13023-019-1151-0},
url = {https://doi.org/10.1186/s13023-019-1151-0}
}RIS
TY - JOUR TI - Pediatric patients with RASopathy-associated hypertrophic cardiomyopathy: the multifaceted consequences of PTPN11 mutations AU - Giulio Calcagni AU - Maria Cristina Digilio AU - Bruno Marino AU - Marco Tartaglia PY - 2019 JO - Orphanet Journal of Rare Diseases DO - 10.1186/s13023-019-1151-0 UR - https://doi.org/10.1186/s13023-019-1151-0 ER -
APA
Calcagni, G., Digilio, M. C., Marino, B., & Tartaglia, M. (2019). Pediatric patients with RASopathy-associated hypertrophic cardiomyopathy: the multifaceted consequences of PTPN11 mutations. Orphanet Journal of Rare Diseases. https://doi.org/10.1186/s13023-019-1151-0
Source records
- crossref · retrieved 2026-11-08T19:05:18.202Z