You are here: vision-research.eu » People » Research Groups » France » Dollfus, Hélène

Pathogenesis and molecular epidemiology of rare genetic disorders

The research group of Hélène Dollfus is working on clinical , molecular and cell biology of inherited syndromic retinitis pigmentosa.

Methodology

  • Clinical research
  • Molecular biology
  • Cell biology

Scientific Cooperations

Group Leader

Hélène Dollfus
[more information]

Contact

Inserm - Université de Strasbourg - Hôpitaux Universitaires de Strasbourg

Faculté de Médecine de Strasbourg,
11 rue Humann
Strasbourg
France

Phone: +33388128120
Fax: +33388128125

Email:
Helene.dollfus[at]medecine.u-strasbg.fr

Current Research Projects

  • Project 1
    Bardet-Bield syndrome
  • Project 2
    Cockayne syndrome

Research Groups

People

Related Research Groups

aging
Oops, an error occurred! Code: 201904200133425519bf81
candidate gene analysis
Oops, an error occurred! Code: 20190420013342ab4f15da
gene/expression
Oops, an error occurred! Code: 20190420013342cc40461d
gene microarray
Oops, an error occurred! Code: 20190420013342499ca9ae
retinitis pigmentosa
Oops, an error occurred! Code: 20190420013342896bacee
Bardet-Bield syndrome
Oops, an error occurred! Code: 20190420013342767d7949
cockayne syndrome
Oops, an error occurred! Code: 201904200133423eb545e5
ciliopathies
Oops, an error occurred! Code: 20190420013342c4f2663b
dna repair
Oops, an error occurred! Code: 20190420013342f51d2305