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Vornweg J, Glaser S, Ahmad-Anwar M, Zimmer AD, et al. Identification of compound heterozygous mutations in AP1B1 leading to the newly-described recessive keratitis-ichthyosis-deafness (KIDAR) syndrome. Br J Dermatol 2021 Jan 16. doi: 10.1111/bjd.19815.
PMID: 33452671


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