A Complex of BBS1 and NPHP7 Is Required for Cilia Motility in Zebrafish

Bardet-Biedl syndrome (BBS) and nephronophthisis (NPH) are hereditary autosomal recessive disorders, encoded by two families of diverse genes. BBS and NPH display several overlapping phenotypes including cystic kidney disease, retinitis pigmentosa, liver fibrosis, situs inversus and cerebellar defec...

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Detaylı Bibliyografya
Asıl Yazarlar: Kim, Yun Hee, Epting, Daniel, Slanchev, Krasimir, Engel, Christina, Walz, Gerd, Kramer-Zucker, Albrecht
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Public Library of Science 2013
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3771994/
https://ncbi.nlm.nih.gov/pubmed/24069149
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0072549
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