Haberberger Birgit: Difference between revisions

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==Participated at==
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Latest revision as of 10:43, 7 September 2018

Name Haberberger Birgit, MSc
Institution Institut fΓΌr Humangenetik

Helmholtz Zentrum MΓΌnchen - Deutsches Forschungszentrum fΓΌr Gesundheit und Umwelt

Address IngolstΓ€dter Landstr. 1, 85764
City Neuherberg
State/Province
Country Germany
Email
Weblink
O2k-Network Lab


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Publications

 PublishedReference
Jackson 2014 J Med Genet2014Jackson CB, Nuoffer JM, Hahn D, Prokisch H, Haberberger B, Gautsch M, HΓ€berli 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 Genet2010Haack 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.

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