NGLY1 Deficiency Zebrafish Model Manifests Abnormalities of the Nervous and Musculoskeletal Systems

Background: NGLY1 is an enigmatic enzyme with multiple functions across a wide range of species. In humans, pathogenic genetic variants in NGLY1 are linked to a variable phenotype of global neurological dysfunction, abnormal tear production, and liver disease presenting the rare autosomal recessive...

Descripción completa

Detalles Bibliográficos
Autores principales: Mesika, Aviv, Nadav, Golan, Shochat, Chen, Kalfon, Limor, Jackson, Karen, Khalaileh, Ayat, Karasik, David, Falik-Zaccai, Tzipora C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9234281/
https://www.ncbi.nlm.nih.gov/pubmed/35769264
http://dx.doi.org/10.3389/fcell.2022.902969

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9234281/
https://www.ncbi.nlm.nih.gov/pubmed/35769264
http://dx.doi.org/10.3389/fcell.2022.902969

Ejemplares similares