Uncovering the gene variants in a global cohort of patients with unexplained increased left ventricular wall thickness using next-generation sequencing

Abstract Background Genetic analysis using massive parallel sequencing is crucial for the accurate and early diagnosis of hereditary hypertrophic cardiomyopathies and their phenocopies, especially transthyretin cardiac amyloidosis (ATTR-CA) and Fabry disease (FD). This study extends the cardio next-...

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التفاصيل البيبلوغرافية

المؤلفون الرئيسيون:	Michael Arad, Andrea Virginia Ferreira Chaves, Murillo Antunes, Abeer Bakhsh, Kenneth I. Berger, Tse Hung Fat, Armando Alves da Fonseca, Adriana Furtado, Irina Maksimova, Sandra Marques e Silva, Manish Maski, Enrique Monjes, Nelson E. Murillo Benitez, Eduardo Ortuño Campos, Márcia Gonçalves Ribeiro, Maria Juliana Rodriguez-González, Wen-Chung Yu, Huseyin Onay
التنسيق:	Artigo
اللغة:	Inglês
منشور في:	BMC 2026-04-01
سلاسل:	BMC Cardiovascular Disorders
الموضوعات:	Next-generation sequencing Left ventricular wall thickness Hypertrophic cardiomyopathy Transthyretin cardiac amyloidosis Fabry disease Alpha-galactosidase A
الوصول للمادة أونلاين:	https://doi.org/10.1186/s12872-026-05834-5
الوسوم:	إضافة وسم لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!