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Albrecht-Kossel-Institute
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Defects in the retina of Niemann-pick type C 1 mutant mice.
BMC neuroscience Nov, 2014 | Pubmed ID: 25472750
A novel, highly sensitive and specific biomarker for Niemann-Pick type C1 disease.
Orphanet journal of rare diseases Jun, 2015 | Pubmed ID: 26082315
The Large Phenotypic Spectrum of Fabry Disease Requires Graduated Diagnosis and Personalized Therapy: A Meta-Analysis Can Help to Differentiate Missense Mutations.
International journal of molecular sciences Dec, 2016 | Pubmed ID: 27916943
Fluorescent probes for selective protein labeling in lysosomes: a case of α-galactosidase A.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology Dec, 2017 | Pubmed ID: 28821638
Glucosylsphingosine Causes Hematological and Visceral Changes in Mice-Evidence for a Pathophysiological Role in Gaucher Disease.
International journal of molecular sciences Oct, 2017 | Pubmed ID: 29053611
University Rostock Medical Center
Jan Lukas1,
Anne-Marie Knospe1,
Susanne Seemann1,
Valentina Citro2,
Maria V. Cubellis2,
Arndt Rolfs1,3
1Albrecht-Kossel-Institute, University Rostock Medical Center,
2Department of Biology, University Federico II,
3, Centogene AG
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