Difference between revisions of "Bianchi L"
From Bioblast
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|lastname=Bianchi | |lastname=Bianchi | ||
|firstname=Lucas | |firstname=Lucas | ||
|institution=nstitut Imagine | |||
DR1 INSERM Génétique des Maladies Mitochondriales | |||
|city=Paris | |city=Paris | ||
|country=France | |country=France | ||
Revision as of 13:00, 9 February 2016
| Name | Bianchi Lucas, |
|---|---|
| Institution | nstitut Imagine
DR1 INSERM Génétique des Maladies Mitochondriales |
| Address | , |
| City | Paris |
| State/Province | |
| Country | France |
| [email protected] | |
| Weblink | |
| O2k-Network Lab |
Labels:
Publications
| Published | Reference | |
|---|---|---|
| Gerber 2016 J Med Genet | 2016 | Gerber S, Ding MG, Gérard X, Zwicker K, Zanlonghi X, Rio M, Serre V, Hanein S, Munnich A, Rotig A, Bianchi L, Amati-Bonneau P, Elpeleg O, Kaplan J, Brandt U, Rozet JM (2016) Compound heterozygosity for severe and hypomorphic NDUFS2 mutations cause non-syndromic LHON-like optic neuropathy. J Med Genet 54:346-56. |
