Identification of circulating miRNAs differentially expressed in patients with Limb-girdle, Duchenne or facioscapulohumeral muscular dystrophies

Abstract Background Limb-girdle muscular dystrophy (LGMD) is a rare neuromuscular disease including a growing and heterogeneous number of subtypes with variable phenotype. Their clinical and histopathological characteristics frequently overlap with other neuromuscular dystrophies. Our goal was to id...

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Asıl Yazarlar:	José Luis García-Giménez, Elena R. García-Trevijano, Ana I. Avilés-Alía, José Santiago Ibañez-Cabellos, Miquel Bovea-Marco, Teresa Bas, Federico V. Pallardó, Juan R. Viña, Rosa Zaragozá
Materyal Türü:	Artigo
Dil:	Inglês
Baskı/Yayın Bilgisi:	BMC 2022-12-01
Seri Bilgileri:	Orphanet Journal of Rare Diseases
Konular:	Limb girdle muscular dystrophies Circulating miRs Molecular signature Duchenne muscular dystrophy Facioscapulohumeral muscular dystrophy
Online Erişim:	https://doi.org/10.1186/s13023-022-02603-3
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