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Juliane Müller
Juliane Müller
University of Newcastle
Ophthalmology
Diabetes mellitus
Congenital myasthenic syndrome
Physical therapy
Medicine
2
Papers
104
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Expanding the Clinical Phenotype of Agrin-Associated Congenital Myasthenic Syndrome
2013
Neurology
Amina Chaouch
T. Torbergsen
Juliane Müller
Kate Bushby
Volker Straub
Angela Abicht
Hanns Lochmüller
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Cytochrome c oxidase deficiency due to mutations in SCO2, encoding a mitochondrial copper-binding protein, is rescued by copper in human myoblasts
2001
Human Molecular Genetics
Michaela Jaksch
Claudia Paret
Rolf Stucka
Nina Horn
J. Müller-Höcker
Rita Horvath
Nadine Trepesch
Gerhard Stecker
Peter Freisinger
Christian Thirion
Juliane Müller
Renate Lunkwitz
Gerhard Rödel
Eric A. Shoubridge
Hanns Lochmüller
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Citations (104)
1