Sebastian Froehler

Sebastian Froehler

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Sebastian Froehler

Sebastian Froehler

Publications by authors named "Sebastian Froehler"

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HDAC4 mutations cause diabetes and induce β-cell FoxO1 nuclear exclusion.

Mol Genet Genomic Med 2019 05 9;7(5):e602. Epub 2019 Apr 9.

Experimental and Clinical Research Center (ECRC), a joint cooperation between the Charité Medical Faculty, Max-Delbrueck-Center for Molecular Medicine (MDC), Berlin, Germany.

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https://onlinelibrary.wiley.com/doi/abs/10.1002/mgg3.602
Publisher Site
http://dx.doi.org/10.1002/mgg3.602DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503015PMC
May 2019

Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation.

Orphanet J Rare Dis 2013 Nov 14;8:178. Epub 2013 Nov 14.

Institute of Cell Biology and Neurobiology, Charité University Medicine Berlin, Campus Virchow-Klinikum, Augustenburger Platz 1, Berlin 13353, Germany.

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http://dx.doi.org/10.1186/1750-1172-8-178DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4225825PMC
November 2013