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Institut für Humangenetik der Universitätsmedizin Göttingen Institut für Humangenetik der Universitätsmedizin Göttingen
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News

Home » News » Page 3
By KB
In News, Research
Posted 13. July 2021

Variants in clustered protocadherin PCDHGC4 identified as genetic cause of novel neurodevelopmental disorder

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By KB
In News, Research
Posted 5. July 2021

Novel homozygous truncating DNM1 variants identified as genetic cause of developmental and epileptic encephalopathy (DEE)

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By KB
In News, Research
Posted 4. June 2021

Göttingen researchers reveal first molecular mechanism underlying the rare Hallermann-Streiff syndrome

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By KB
In News
Posted 22. April 2021

A novel center specifically targeting disorders with premature ageing at the Institute of Human Genetics

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By KB
In News, Research
Posted 25. February 2021

Recently published review article on premature ageing disorders

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By KB
In News, Research
Posted 26. January 2021

Variants in SUFU gene cause congenital eye movement disorder

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By KB
In News, Research
Posted 19. January 2021

CRISPR genome editing: A clinically translatable strategy to treat heart disease

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By KB
In News, Research
Posted 7. October 2020

Developing personalized therapy strategies for pancreatic cancer: UMG receives DFG funding

Developing new and specific therapeutic options for pancreatic cancer (PDAC) is the overall goal of a new Clinical Research Unit at the University Medical Center Göttingen, to which the German [...]

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By KB
In News, Research
Posted 16. June 2020

Common genetic cause of unclear disorder in three children uncovered

Researchers at the Institute of Human Genetics Göttingen have uncovered the genetic cause of a previously undescribed disorder associated with a combination of several malformations and [...]

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By KB
In News, Research
Posted 11. October 2019

Brittle bone disease: Novel gene provides clue to potential therapeutic approach in the future

Extremely fragile bones are the reason why mainly children, but also adults with brittle bone disease will frequently break their bones, often even without any apparent injury. The genetic [...]

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