Cargando…
IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy phenotype
BACKGROUND: Bidirectional intraflagellar transport (IFT) consists of two major protein complexes, IFT-A and IFT-B. In contrast to the IFT-B complex, all components of IFT-A have recently been linked to human ciliopathies when defective. We therefore hypothesised that mutations in additional IFT-B en...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4621372/ https://www.ncbi.nlm.nih.gov/pubmed/26275418 http://dx.doi.org/10.1136/jmedgenet-2014-102838 |