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

Published in:

British Journal of Dermatology, 2021, v. 184, n. 6, p. 1190, doi. 10.1111/bjd.19815

By:

• Vornweg, J.;
• Gläser, S.;
• Ahmad‐Anwar, M.;
• Zimmer, A.D.;
• Kuhn, M.;
• Hörer, S.;
• Korenke, G.C.;
• Grothaus, J.;
• Ott, H.;
• Fischer, J.

Publication type:

Article