Pediatric patients with RASopathy-associated hypertrophic cardiomyopathy: the multifaceted consequences of PTPN11 mutations.

Calcagni G, Digilio MC, Marino B, Tartaglia M

DOI: 10.1186/s13023-019-1151-0
Published: 2019 Jul 5
Container: Orphanet journal of rare diseases
Publisher: Not recorded
Open access: yes

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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 = {Calcagni G and Digilio MC and Marino B and Tartaglia M},
  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  - Calcagni G
AU  - Digilio MC
AU  - Marino B
AU  - Tartaglia M
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

G, C., MC, D., B, M., & M, T. (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

pubmed · retrieved 2026-09-25T21:09:23.146Z