Sabine Jägle
3PUBLICATIONS
6CO-AUTHORS
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Publications (3)
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|Jan 23, 2023
Pathogenic variants in the SPTLC1 gene cause hyperkeratosis lenticularis perstans.Sabine Jägle, Hao-Hsiang Hsu, Hazem A Juratli
|Nov 27, 2021
Marfan Syndrome Caused by Disruption of the FBN1 Gene due to A Reciprocal Chromosome Translocation.Anna Clara Schnause, Katalin Komlosi, Barbara Herr
|Aug 09, 2020
Recurrent MVD mutation in European patients with disseminated porokeratosis.M Saleva-Stateva, K Technau-Hafsi, L Frommherz
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