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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Principais autores:	Yun Hee Kim, Daniel Epting, Krasimir Slanchev, Christina Engel, Gerd Walz, Albrecht Kramer-Zucker
格式:	Artigo
語言:	Inglês
出版:	Public Library of Science (PLoS) 2013-01-01
叢編:	PLoS ONE
在線閱讀:	http://europepmc.org/articles/PMC3771994?pdf=render
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