Difference between revisions of "Bianchi L"
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{{Person}} | {{Person | ||
|lastname=Bianchi | |||
|firstname=Lucas | |||
|institution=Institut Imagine | |||
DR1 INSERM Génétique des Maladies Mitochondriales | |||
|city=Paris | |||
|country=France | |||
}} | |||
{{Labelingperson}} | |||
== Participated 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 | |
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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. |