Difference between revisions of "Bianchi L"
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|lastname=Bianchi | |lastname=Bianchi | ||
|firstname=Lucas | |firstname=Lucas | ||
|institution= | |institution=Institut Imagine | ||
DR1 INSERM Génétique des Maladies Mitochondriales | DR1 INSERM Génétique des Maladies Mitochondriales | ||
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== Participated at == | == Participated at == | ||
* [[MiPNet21.01 IOC109 Schroecken AT| IOC109 Schroecken AT]] | ::::* [[MiPNet21.01 IOC109 Schroecken AT| IOC109 Schroecken AT]] | ||
Latest revision as of 12:16, 14 February 2018
| Name | Bianchi Lucas, |
|---|---|
| Institution | Institut 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. |
