Addgene: Molecular basis of ciliary defects caused by compound heterozygous IFT144/WDR19 mutations found in cranioectodermal dysplasia.

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Kazuhisa Nakayama
Ishida et al

Molecular basis of ciliary defects caused by compound heterozygous IFT144/WDR19 mutations found in cranioectodermal dysplasia.
Ishida Y, Kobayashi T, Chiba S, Katoh Y, Nakayama K
Hum Mol Genet. 2021 Apr 26;30(3-4):213-225. doi: 10.1093/hmg/ddab034. PubMed Article

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ID	Plasmid	Purpose
162276	pGEX6P1-mCherry-Nanobody (LaM-2)	Expresses GST-tagged anti-mCherry Nanobody (LaM-2) in E. coli cells.

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