Old Web
English
Sign In
Acemap
>
authorDetail
>
Sebastian Froehler
Sebastian Froehler
Max Delbrück Center for Molecular Medicine
Biology
Genetics
Centrosome
Heterozygote advantage
Compound heterozygosity
2
Papers
33
Citations
0.00
KQI
Citation Trend
Filter By
Interval:
1900~2024
1900
2024
Author
Papers (2)
Sort By
Default
Most Recent
Most Early
Most Citation
No data
Journal
Conference
Others
HDAC4 mutations cause diabetes and induce β‐cell FoxO1 nuclear exclusion
2019
Molecular Genetics & Genomic Medicine
Maolian Gong
Yong Yu
Lei Liang
Dogus Vuralli
Sebastian Froehler
Peter Kuehnen
Philipp Du Bois
Jingjing Zhang
Aidi Cao
Yuantao Liu
Khalid Hussain
Jens Fielitz
Shiqi Jia
Wei Chen
Klemens Raile
Show All
Source
Cite
Save
Citations (7)
Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation
2013
Orphanet Journal of Rare Diseases
Heba Gamal Farag
Sebastian Froehler
Konrad Oexle
Ethiraj Ravindran
Detlev Schindler
Timo Staab
Angela Huebner
Nadine Kraemer
Wei Chen
Angela M. Kaindl
Show All
Source
Cite
Save
Citations (26)
1