FLNC-Associated Myofibrillar Myopathy

Por um escritor misterioso
Last updated 19 novembro 2024
FLNC-Associated Myofibrillar Myopathy
FLNC-Associated Myofibrillar Myopathy
FLNC Gene - GeneCards, FLNC Protein
FLNC-Associated Myofibrillar Myopathy
Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies - ScienceDirect
FLNC-Associated Myofibrillar Myopathy
A mutation update for the FLNC gene in myopathies and cardiomyopathies - Verdonschot - 2020 - Human Mutation - Wiley Online Library
FLNC-Associated Myofibrillar Myopathy
Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies
FLNC-Associated Myofibrillar Myopathy
A mutation in the filamin c gene causes myofibrillar myopathy with lower motor neuron syndrome: a case report, BMC Neurology
FLNC-Associated Myofibrillar Myopathy
Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood, Orphanet Journal of Rare Diseases
FLNC-Associated Myofibrillar Myopathy
PDF) A Mutation Update for the FLNC gene in Myopathies and Cardiomyopathies
FLNC-Associated Myofibrillar Myopathy
Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies – topic of research paper in Basic medicine. Download scholarly article PDF and read for free on CyberLeninka open science hub.
FLNC-Associated Myofibrillar Myopathy
Filamin C regulates skeletal muscle atrophy by stabilizing dishevelled-2 to inhibit autophagy and mitophagy - ScienceDirect
FLNC-Associated Myofibrillar Myopathy
Novel Mutation in FLNC (Filamin C) Causes Familial Restrictive Cardiomyopathy
FLNC-Associated Myofibrillar Myopathy
JCM, Free Full-Text

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