Title |
Identification of compound heterozygous mutations in AP1B1 leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome |
|---|---|
Involved |
Julia Keller (Verfasser)
Selina Gläser (Verfasser) Mewish Ahmad‐Anwar (Verfasser) Andreas D. Zimmer (Verfasser)
Marion Kuhn (Verfasser)
Steffen Hörer (Verfasser) Christoph Korenke (Verfasser) Julia Grothaus (Verfasser) Hagen Ott (Verfasser) Judith Fischer (Verfasser) |
Published |
Freiburg: Universität |
Extent |
Online-Ressource |
Language |
|
Country |
|
Topic |
|
Subject |
Dermatology |
DDC notation |
|
Persistent identifier |
urn:nbn:de:bsz:25-freidok-1939336 (URN) |
Further information |
British journal of dermatology. - 184, 6 (2021) , 1190-1192, ISSN: 1365-2133 |
Record ID |
1246678780 |
Please note
The beta version does not yet contain all functions and information of the DNB portal catalogue. If you are missing information or want to order a medium, please visit the page in the DNB portal catalogue via the following link: