Haberberger Birgit: Difference between revisions
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|address=Ingolstädter Landstr. 1 | |address=Ingolstädter Landstr. 1 | ||
|area code=85764 | |area code=85764 | ||
|city=Neuherberg | |city=Neuherberg | ||
|country=Germany | |||
}} | }} | ||
{{Labelingperson}} | {{Labelingperson}} | ||
==Participated at== | |||
:::: [[IOC50]] | |||
Revision as of 14:30, 1 June 2017
| Name | Haberberger Birgit, MSc |
|---|---|
| Institution | Institut für Humangenetik
Helmholtz Zentrum München - Deutsches Forschungszentrum für Gesundheit und Umwelt |
| Address | Ingolstädter Landstr. 1, 85764 |
| City | Neuherberg |
| State/Province | |
| Country | Germany |
| Weblink | |
| O2k-Network Lab |
Labels:
Publications
| Published | Reference | |
|---|---|---|
| Jackson 2014 J Med Genet | 2014 | Jackson CB, Nuoffer JM, Hahn D, Prokisch H, Haberberger B, Gautsch M, Häberli 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. |
| Haack 2010 Nat Genet | 2010 | Haack TB, Danhauser K, Haberberger B, Hoser J, Strecker V, Boehm D, Uziel G, Lamantea E, Invernizzi F, Poulton J, Rolinski B, Iuso A, Biskup S, Schmidt T, Mewes HW, Wittig I, Meitinger T, Zeviani M, Prokisch H (2010) Exome sequencing identifies ACAD9 mutations as a cause of Complex I deficiency. Nat Genet 42:1131-4. |
