DE Munich Prokisch H: Difference between revisions

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<nowiki> {{MiPNetLab
<nowiki> {{O2k-Network Lab
|institution=Institut fรผr Humangenetik
|institution=Institut fรผr Humangenetik, Helmholtz Zentrum Mรผnchen - Deutsches Forschungszentrum fรผr Gesundheit und Umwelt
Helmholtz Zentrum Mรผnchen -
Deutsches Forschungszentrum fรผr Gesundheit und Umwelt
|address=Ingolstรคdter Landstr. 1
|address=Ingolstรคdter Landstr. 1
|area code=85764
|area code=85764
Line 9: Line 7:
|Contact=Prokisch Holger
|Contact=Prokisch Holger
|MiPNetLab=Ahting Uwe, Arduino Daniela M. Haberberger Birgit, Hierl Konrad, Iuso Arcangela, Schiller Evelyn, Tripathi Utkarsh, Zeh Ramona
|MiPNetLab=Ahting Uwe, Arduino Daniela M. Haberberger Birgit, Hierl Konrad, Iuso Arcangela, Schiller Evelyn, Tripathi Utkarsh, Zeh Ramona
|Team previous=
|Status=[[http://www.oroboros.at/?Power-O2k '''2 Power-O2k''']] 2006-
|Status=[[http://www.oroboros.at/?Power-O2k '''2 Power-O2k''']] 2006-
|info=
}}
}}

Revision as of 12:47, 4 March 2015

<nowiki>

                



DE Munich Prokisch H

Oroboros O2k-Network

O2k-Network
O2k-Network Lab Institut fรผr Humangenetik, Helmholtz Zentrum Mรผnchen - Deutsches Forschungszentrum fรผr Gesundheit und Umwelt
Address Ingolstรคdter Landstr. 1, 85764
City Neuherberg
State/Prov
Country Germany
Weblink
Contact Prokisch Holger
Team Ahting Uwe, Arduino Daniela M. Haberberger Birgit, Hierl Konrad, Iuso Arcangela, Schiller Evelyn, Tripathi Utkarsh, Zeh Ramona
Team previous
Status [2 Power-O2k] 2006-
Oroboros Events
Topics


O2k-Publications

 PublishedReference
Jackson 2014 J Med Genet2014Jackson CB, Nuoffer JM, Hahn D, Prokisch H, Haberberger B, Gautsch M, Hรคberli A, Gallati S, Schaller A (2014) Mutations in SDHD lead to autosomal recessive encephalomyopathy and isolated mitochondrial Complex II deficiency. J Med Genet 51:170-5.

O2k-Abstracts

update please

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