Identification of compound heterozygous mutations in AP1B1 leading to the newly described recessive keratitis-ichthyosis-deafness (KIDAR) syndrome

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Bibliographic Details
Published inThe British journal of dermatology Vol. 184; no. 6; pp. 1190 - 1192
Main Authors Vornweg, J, Gläser, S, Ahmad-Anwar, M, Zimmer, A D, Kuhn, M, Hörer, S, Korenke, G C, Grothaus, J, Ott, H, Fischer, J
Format Report
LanguageEnglish
Published 01.06.2021
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ISSN:1365-2133
DOI:10.1111/bjd.19815