FLNC-Associated Myofibrillar Myopathy
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A mutation update for the FLNC gene in myopathies and cardiomyopathies - Verdonschot - 2020 - Human Mutation - Wiley Online Library
First clinical and myopathological description of a myofibrillar myopathy with congenital onset and homozygous mutation in FLNC - Kölbel - 2020 - Human Mutation - Wiley Online Library
Homozygous expression of the myofibrillar myopathy-associated p.W2710X filamin C variant reveals major pathomechanisms of sarcomeric lesion formation, Acta Neuropathologica Communications
New mutation of the desmin gene identified in an extended Indian pedigree presenting with distal myopathy and cardiac disease – topic of research paper in Clinical medicine. Download scholarly article PDF and
Genetic Mutations and Demographic, Clinical, and Morphological Aspects of Myofibrillar Myopathy in a French Cohort
Expanding the central nervous system disease spectrum associated with FLNC mutation - Previtali - 2019 - Muscle & Nerve - Wiley Online Library
Cells, Free Full-Text
FLNC Antibody (NBP1-89300): Novus Biologicals
Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies - ScienceDirect
FLNC-Associated Myofibrillar Myopathy
FLNC-Associated Myofibrillar Myopathy
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