Identification des mutations responsables de la NHSA2 et de l'AOA2 dans la population canadienne-française : deux nouveaux exemples de maladies à effet fondateur au Québec
| dc.contributor.advisor | Brais, Bernard | |
| dc.contributor.author | Roddier, Katel | |
| dc.date.accessioned | 2016-09-21T20:04:34Z | |
| dc.date.available | 2016-09-21T20:04:34Z | |
| dc.date.issued | 2006 | |
| dc.date.submitted | 2005 | |
| dc.identifier.uri | http://hdl.handle.net/1866/15578 | |
| dc.subject | Génétique | |
| dc.subject | Autosomique récessif | |
| dc.subject | Étude de liaison | |
| dc.subject | Effet fondateur | |
| dc.subject | Québec | |
| dc.subject | Névrite sensitive | |
| dc.subject | Ataxie cérébelleuse | |
| dc.subject | HSN2 | |
| dc.subject | SETX | |
| dc.title | Identification des mutations responsables de la NHSA2 et de l'AOA2 dans la population canadienne-française : deux nouveaux exemples de maladies à effet fondateur au Québec | |
| dc.type | Thèse ou mémoire / Thesis or Dissertation | |
| etd.degree.discipline | Biologie moléculaire | fr |
| etd.degree.grantor | Université de Montréal | fr |
| etd.degree.level | Maîtrise / Master's | |
| etd.degree.name | M. Sc. | |
| dcterms.description | Mémoire numérisé par la Direction des bibliothèques de l'Université de Montréal. | fr |
| dcterms.language | fra |
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