학술논문
Loss of CBY1 results in a ciliopathy characterized by features of Joubert syndrome
Document Type
Article
Author
Epting, D.; Ott, E.; Bergmann, C.; Senaratne, L.D.S.; Holmgren, A.; Sumathipala, D.; Barøy, T.; Frengen, E.; Misceo, D.; Larsen, S.M.; Crowley, S.; Strømme, P.; Wallmeier, J.; Bracht, D.; Omran, H.; Frikstad, K.-A.M.; Patzke, S.; Sikiric, A.; Käsmann-Kellner, B.; Decker, E.; Decker, C.; Bachmann, N.; Phelps, I.G.; Doherty, D.; Katsanis, N.; Davis, E.E.; Giles, R.; Schmidts, M.; Zucknick, M.; Lienkamp, S.S.
Source
In: Human Mutation . (Human Mutation, December 2020, 41(12):2179-2194)
Subject
Language
English
ISSN
10981004
10597794
10597794