Mouse model of severe recessive RYR1-related myopathy

Ryanodine receptor type I (RYR1)-related myopathies (RYR1 RM) are a clinically and histopathologically heterogeneous group of conditions that represent the most common subtype of childhood onset non-dystrophic muscle disorders. There are no treatments for this severe group of diseases. A major barri...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Hum Mol Genet
Hauptverfasser: Brennan, Stephanie, Garcia-Castañeda, Maricela, Michelucci, Antonio, Sabha, Nesrin, Malik, Sundeep, Groom, Linda, Wei LaPierre, Lan, Dowling, James J, Dirksen, Robert T
Format: Artigo
Sprache:Inglês
Veröffentlicht: Oxford University Press 2019
Schlagworte:
General Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6737254/
https://ncbi.nlm.nih.gov/pubmed/31107960
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddz105
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!

Ähnliche Einträge