FLNC-Associated Myofibrillar Myopathy
Por um escritor misterioso
Descrição
Filamin C-related myopathies: pathology and mechanisms
FLNC and MYLK2 gene mutations in a Chinese family with different phenotypes of cardiomyopathy
Cells, Free Full-Text
Cells, Free Full-Text
Filamin C (FLNC) – Equiseq
Clinical and pathological characterization of FLNC‐related myofibrillar myopathy caused by founder variant c.8129G>A in Hong Kong Chinese - Lee - 2020 - Clinical Genetics - Wiley Online Library
Aciculin interacts with Xin and FLNc in areas of myofibrillar damage
Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy
FLNC-Associated Myofibrillar Myopathy
Expanding the central nervous system disease spectrum associated with FLNC mutation - Previtali - 2019 - Muscle & Nerve - Wiley Online Library
FLNC and MYLK2 gene mutations in a Chinese family with different phenotypes of cardiomyopathy
PDF) FLNC-Associated Myofibrillar Myopathy: New Clinical, Functional, and Proteomic Data
Main characteristics of filaminopathies
Structure of the FLNC gene and filamin C protein. (a) Within the human
A mutation in the dimerization domain of filamin c causes a novel type of autosomal dominant myofibrillar myopathy.
de
por adulto (o preço varia de acordo com o tamanho do grupo)
