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Published in British journal of dermatology (1951) (01.06.2021)
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Identification of compound heterozygous mutations in AP1B1 leading to the newly described recessive keratitis-ichthyosis-deafness (KIDAR) syndrome
Vornweg, J, Gläser, S, Ahmad-Anwar, M, Zimmer, A D, Kuhn, M, Hörer, S, Korenke, G C, Grothaus, J, Ott, H, Fischer, J
Published in The British journal of dermatology (01.06.2021)
Published in The British journal of dermatology (01.06.2021)
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