Dync2li1-flox 基因敲除小鼠

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3. Aubert-Mucca, Marion, Huber, Céline, Baujat, Genevieve, Attie-Bitach, Tania, Cormier-Daire, Valerie. 2022. Ellis-Van Creveld Syndrome: Clinical and Molecular Analysis of 50 Individuals. In Journal of medical genetics, 60, 337-345. doi:10.1136/jmg-2022-108435. https://pubmed.ncbi.nlm.nih.gov/35927022/

4. Niceta, M, Margiotti, K, Digilio, M C, De Luca, A, Tartaglia, M. 2018. Biallelic mutations in DYNC2LI1 are a rare cause of Ellis-van Creveld syndrome. In Clinical genetics, 93, 632-639. doi:10.1111/cge.13128. https://pubmed.ncbi.nlm.nih.gov/28857138/