Identification of compound heterozygous mutations in AP1B1 leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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British journal of dermatology. - 184, 6 (2021) , 1190-1192, ISSN: 1365-2133
- Ereignis
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Veröffentlichung
- (wo)
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Freiburg
- (wer)
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Universität
- (wann)
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2021
- Urheber
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Keller, Julia
Gläser, Selina
Ahmad‐Anwar, Mewish
Zimmer, Andreas D.
Kuhn, Marion
Hörer, Steffen
Korenke, Christoph
Grothaus, Julia
Ott, Hagen
Fischer, Judith
- DOI
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10.1111/bjd.19815
- URN
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urn:nbn:de:bsz:25-freidok-1939336
- Rechteinformation
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Kein Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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15.08.2025, 07:36 MESZ
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Beteiligte
- Keller, Julia
- Gläser, Selina
- Ahmad‐Anwar, Mewish
- Zimmer, Andreas D.
- Kuhn, Marion
- Hörer, Steffen
- Korenke, Christoph
- Grothaus, Julia
- Ott, Hagen
- Fischer, Judith
- Universität
Entstanden
- 2021
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