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- 2019
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Mark
Biallelic KRT5 mutations in autosomal recessive epidermolysis bullosa simplex, including a complete human keratin 5 “knock-out”
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- Contribution to journal › Article
- 2017
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Mark
Mutations in SULT2B1 Cause Autosomal-Recessive Congenital Ichthyosis in Humans
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- Contribution to journal › Article
- 2015
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Mark
Idiopathic Angioedema and Urticarial Vasculitis in a Patient with a History of Acquired Haemophilia.
(
- Contribution to journal › Article
- 2013
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Mark
Sensitization to Skin-associated Microorganisms in Adult Patients with Atopic Dermatitis is of Importance for Disease Severity.
(
- Contribution to journal › Article