FLNC-Associated Myofibrillar Myopathy
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FLNC-Associated Myofibrillar Myopathy
Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy
FLNC-Associated Myofibrillar Myopathy
Frontiers Case Reports: Novel Missense Variants in the Filamin C Actin Binding Domain Cause Variable Phenotypes
FLNC Antibody (NBP1-89300): Novus Biologicals
Cells, Free Full-Text
FLNC and MYLK2 gene mutations in a Chinese family with different phenotypes of cardiomyopathy
FLNC-Associated Myofibrillar Myopathy
Cureus, DES c.1360C>T: A Rare Desmin Variant Causing Early Distal Myopathy and Cardiomyopathy
First clinical and myopathological description of a myofibrillar myopathy with congenital onset and homozygous mutation in FLNC - Kölbel - 2020 - Human Mutation - Wiley Online Library
FLNC Gene Splice Mutations Cause Dilated Cardiomyopathy - ScienceDirect
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