OpenURL Connection Search - EBSCO

Connecting you to content on EBSCOhostUNIVERSITÄT DORTMUND

Select item for more details and to access through your institution.

A novel nonsense variant in <italic>REEP6</italic> is involved in a sporadic rod‐cone dystrophy case.
Published in:
Clinical Genetics, 2018, v. 93, n. 3, p. 707, doi. 10.1111/cge.13171
By:
- Méjécase, C.;
- Mohand‐saïd, S.;
- El Shamieh, S.;
- Antonio, A.;
- Condroyer, C.;
- Blanchard, S.;
- Letexier, M.;
- Saraiva, J.‐p.;
- Sahel, J.‐a.;
- Audo, I.;
- Zeitz, C.
Publication type:
Article
ARL2BP mutations account for 0.1% of autosomal recessive rod-cone dystrophies with the report of a novel splice variant.
Published in:
Clinical Genetics, 2017, v. 92, n. 1, p. 109, doi. 10.1111/cge.12909
By:
- Audo, I.;
- El Shamieh, S.;
- Méjécase, C.;
- Michiels, C.;
- Demontant, V.;
- Antonio, A.;
- Condroyer, C.;
- Boyard, F.;
- Letexier, M.;
- Saraiva, J.‐P.;
- Blanchard, S.;
- Mohand‐Saïd, S.;
- Sahel, J.‐A.;
- Zeitz, C.
Publication type:
Article
The risk of suicidal behaviour in individuals with psoriasis: A retrospective cohort study in Quebec, Canada.
Published in:
Journal of the European Academy of Dermatology & Venereology, 2020, v. 34, n. 12, p. e800, doi. 10.1111/jdv.16647
By:
- Laverde‐Saad, A.;
- Milan, R.;
- Mohand‐Saïd, S.;
- LeLorier, J.;
- Litvinov, I.V.;
- Rahme, E.
Publication type:
Article