Lessons From a Genotype-Phenotype Study About the Clinical Spectrum of Hypertrophic Cardiomyopathy Associated With Noonan Syndrome With Multiple Lentigines and PTPN11-Mutations
Author:
Affiliation:
1. Institute of Clinical Specialties, Sahlgrenska Academy, Gothenburg University & Children´s Heart Center, Queen Silvia Children´s Hospital, Sahlgrenska University Hospital, Region Västra Götaland, Gothenburg, Sweden.
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference19 articles.
1. Predictors of risk for sudden death in childhood hypertrophic cardiomyopathy: the importance of the ECG risk score
2. Clinical and mutation profile of pediatric patients with RASopathy-associated hypertrophic cardiomyopathy: results from a Chinese cohort
3. Clinical presentation and survival of childhood hypertrophic cardiomyopathy: a retrospective study in United Kingdom
4. Age- and gender-specific mortality rates in childhood hypertrophic cardiomyopathy
5. Long-term outcomes of childhood onset Noonan compared to sarcomere hypertrophic cardiomyopathy
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