Publication | Open Access
Novel ALPK3 mutation in a Tunisian patient with pediatric cardiomyopathy and facio-thoraco-skeletal features
29
Citations
11
References
2018
Year
CardiomyopathyPediatric Heart DiseasePathologyPediatric CardiomyopathyCongenital Heart DefectCongenital Heart AnomalyTunisian PatientMedicineCardiologyNovel Alpk3 MutationCardiovascular Genetics
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