Julia Vornweg
2PUBLICATIONS
5CO-AUTHORS
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Publications (2)
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|Feb 03, 2021
A novel SPINK5 donor splice site variant in a child with Netherton syndrome.Dillon Mintoff, Isabella Borg, Julia Vornweg
|Jan 16, 2021
Identification of compound heterozygous mutations in AP1B1 leading to the newly described recessive keratitis-ichthyosis-deafness (KIDAR) syndrome.J Vornweg, S Gläser, M Ahmad-Anwar
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