Musculoskeletal defects associated with myosin heavy chain‐embryonic loss of function are mediated by the YAP signaling pathway

Mutations in MYH3, the gene encoding the developmental myosin heavy chain‐embryonic (MyHC‐embryonic) skeletal muscle‐specific contractile protein, cause several congenital contracture syndromes. Among these, recessive loss‐of‐function MYH3 mutations lead to spondylocarpotarsal synostosis (SCTS), cha...

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Detalles Bibliográficos
Autores principales: Bharadwaj, Anushree, Sharma, Jaydeep, Singh, Jagriti, Kumari, Mahima, Dargar, Tanushri, Kalita, Bhargab, Mathew, Sam J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10493586/
https://www.ncbi.nlm.nih.gov/pubmed/37492882
http://dx.doi.org/10.15252/emmm.202217187

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10493586/
https://www.ncbi.nlm.nih.gov/pubmed/37492882
http://dx.doi.org/10.15252/emmm.202217187

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