| 标题 |
Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish |
| 网址 | |
| DOI | |
| 其它 |
期刊:The American Journal of Human Genetics 作者:Julie C. Van De Weghe; Tamara D.S. Rusterholz; Brooke Latour; Megan E. Grout; Kimberly A. Aldinger; et al 出版日期:2017 |
| 求助人 | |
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(2025-6-4)