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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
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- Article
Paediatric lichen sclerosus: a systematic review of 4516 cases.
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- British Journal of Dermatology, 2020, v. 182, n. 1, p. 231, doi. 10.1111/bjd.18267
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- Publication type:
- Article
Das rote, schuppende Baby: ein kinderdermatologischer Notfall.
- Published in:
- Der Hautarzt, 2017, v. 68, n. 10, p. 796, doi. 10.1007/s00105-017-4035-z
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- Article