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Jump to: 2020
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2020

Cesarato, N., Malki, L., Sarig, O., Mohamad, J., Canter, T., Assaf, S., Pavlovsky, M., Vodo, D., Anis, Y., Bihari, O., Malovitski, K., Gat, A., Thiele, H., White, B. E. Perez, Samuelov, L., Nanda, A., Paller, A. S., Betz, R. C. and Sprecher, E. (2020). Loss-of-function variants in C3ORF52 result in localized autosomal recessive hypotrichosis. Eur. J. Hum. Genet., 28 (SUPPL 1). S. 233 - 235. LONDON: SPRINGERNATURE. ISSN 1476-5438

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