Cargando…
Biallelic variants in COPB1 cause a novel, severe intellectual disability syndrome with cataracts and variable microcephaly
BACKGROUND: Coat protein complex 1 (COPI) is integral in the sorting and retrograde trafficking of proteins and lipids from the Golgi apparatus to the endoplasmic reticulum (ER). In recent years, coat proteins have been implicated in human diseases known collectively as “coatopathies”. METHODS: Whol...
Autores principales: | Macken, William L., Godwin, Annie, Wheway, Gabrielle, Stals, Karen, Nazlamova, Liliya, Ellard, Sian, Alfares, Ahmed, Aloraini, Taghrid, AlSubaie, Lamia, Alfadhel, Majid, Alajaji, Sulaiman, Wai, Htoo A., Self, Jay, Douglas, Andrew G. L., Kao, Alexander P., Guille, Matthew, Baralle, Diana |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7908744/ https://www.ncbi.nlm.nih.gov/pubmed/33632302 http://dx.doi.org/10.1186/s13073-021-00850-w |
Ejemplares similares
-
DeepSVP: integration of genotype and phenotype for structural variant prioritization using deep learning
por: Althagafi, Azza, et al.
Publicado: (2021) -
Common disease-associated gene variants in a Saudi Arabian population
por: Aleissa, Mariam, et al.
Publicado: (2022) -
Signaling through the Primary Cilium
por: Wheway, Gabrielle, et al.
Publicado: (2018) -
Biallelic mutations in UGDH cause congenital microcephaly
por: Shu, Li, et al.
Publicado: (2023) -
661W Photoreceptor Cell Line as a Cell Model for Studying Retinal Ciliopathies
por: Wheway, Gabrielle, et al.
Publicado: (2019)