Cargando…
Autosomal recessive variants in TUBGCP2 alter the γ-tubulin ring complex leading to neurodevelopmental disease
Microtubules help building the cytoskeleton of neurons and other cells. Several components of the gamma-tubulin (γ-tubulin) complex have been previously reported in human neurodevelopmental diseases. We describe two siblings from a consanguineous Turkish family with dysmorphic features, developmenta...
Autores principales: | Gungor, Serdal, Oktay, Yavuz, Hiz, Semra, Aranguren-Ibáñez, Álvaro, Kalafatcilar, Ipek, Yaramis, Ahmet, Karaca, Ezgi, Yis, Uluc, Sonmezler, Ece, Ekinci, Burcu, Aslan, Mahmut, Yilmaz, Elmasnur, Özgör, Bilge, Balaraju, Sunitha, Szabo, Nora, Laurie, Steven, Beltran, Sergi, MacArthur, Daniel G., Hathazi, Denisa, Töpf, Ana, Roos, Andreas, Lochmuller, Hanns, Vernos, Isabelle, Horvath, Rita |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7797523/ https://www.ncbi.nlm.nih.gov/pubmed/33458610 http://dx.doi.org/10.1016/j.isci.2020.101948 |
Ejemplares similares
-
Severe neurodevelopmental disease caused by a homozygous TLK2 variant
por: Töpf, Ana, et al.
Publicado: (2019) -
COL4A1-related autosomal recessive encephalopathy in 2 Turkish children
por: Yaramis, Ahmet, et al.
Publicado: (2020) -
High diagnostic rate of trio exome sequencing in consanguineous families with neurogenetic diseases
por: Hiz Kurul, Semra, et al.
Publicado: (2021) -
Confirmation of TACO1 as a Leigh Syndrome Disease Gene in Two Additional Families
por: Oktay, Yavuz, et al.
Publicado: (2020) -
Parieto-occipital encephalomalacia in children; clinical and electrophysiological features of twenty-seven cases
por: Karaoğlu, Pakize, et al.
Publicado: (2015)