Human molecular genetics, 2014-01, Vol.23 (2), p.491-501
- Audo, Isabelle
- Bujakowska, Kinga
- Orhan, Elise
- El Shamieh, Said
- Sennlaub, Florian
- Guillonneau, Xavier
- Antonio, Aline
- Michiels, Christelle
- Lancelot, Marie-Elise
- Letexier, Melanie
- Saraiva, Jean-Paul
- Nguyen, Hoan
- Luu, Tien D.
- Léveillard, Thierry
- Poch, Olivier
- Dollfus, Hélène
- Paques, Michel
- Goureau, Olivier
- Mohand-Saïd, Saddek
- Bhattacharya, Shomi S.
- Sahel, José-Alain
- Zeitz, Christina
2014
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- Autor(en) / Beteiligte
- Audo, Isabelle
- Bujakowska, Kinga
- Orhan, Elise
- El Shamieh, Said
- Sennlaub, Florian
- Guillonneau, Xavier
- Antonio, Aline
- Michiels, Christelle
- Lancelot, Marie-Elise
- Letexier, Melanie
- Saraiva, Jean-Paul
- Nguyen, Hoan
- Luu, Tien D.
- Léveillard, Thierry
- Poch, Olivier
- Dollfus, Hélène
- Paques, Michel
- Goureau, Olivier
- Mohand-Saïd, Saddek
- Bhattacharya, Shomi S.
- Sahel, José-Alain
- Zeitz, Christina
- Titel
- The familial dementia gene revisited: a missense mutation revealed by whole-exome sequencing identifies ITM2B as a candidate gene underlying a novel autosomal dominant retinal dystrophy in a large family
- Ist Teil von
- Human molecular genetics, 2014-01, Vol.23 (2), p.491-501
- Erscheinungsjahr
- 2014
- Quelle
- Electronic Journals Library
- Sprache
- Englisch
- Identifikatoren
- ISSN: 0964-6906eISSN: 1460-2083DOI: 10.1093/hmg/ddt439Titel-ID: cdi_crossref_primary_10_1093_hmg_ddt439
- Format
- –