Author Korenke, G. Christoph
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2014 | Journal Article |
High mutation detection rates in cerebral cavernous malformation upon stringent inclusion criteria: one-third of probands are minors.
Spiegler, S.; Najm, J.; Liu, J.; Gkalympoudis, S.; Schröder, W.; Borck, G. & Brockmann, K. et al. (2014)
Molecular genetics & genomic medicine, 2(2) pp. 176-185. DOI: https://doi.org/10.1002/mgg3.60
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2016 | Journal Article
Constitutional de novo and postzygotic mutations in isolated cases of cerebral cavernous malformations
Rath, M.; Spiegler, S.; Nath, N.; Schwefel, K.; Di Donato, N.; Gerber, J. & Korenke, G. C. et al. (2016)
Molecular Genetics & Genomic Medicine, 5(1) pp. 21-27. DOI: https://doi.org/10.1002/mgg3.256
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2019 | Journal Article |
Severe neonatal multiple sulfatase deficiency presenting with hydrops fetalis in a preterm birth patient
Schlotawa, L.; Dierks, T.; Christoph, S.; Cloppenburg, E.; Ohlenbusch, A.; Korenke, G. C. & Gärtner, J. (2019)
JIMD Reports, 49(1) pp. 48-52. DOI: https://doi.org/10.1002/jmd2.12074
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