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Ulrich Müller

Research Profile

Physiology

Chemicals & Drugs

Shaw Potassium Channels

Disorders

Concepts & Ideas

Anatomy

Chromosomes, Human, Pair 19

Geographic Areas

Philippines

Genes & Molecular Sequences

Dominant Genes

Living Beings

Xenopus laevis

Procedures

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Co-author Network

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Publications

TOP 3
Michael F Waters; Natali A Minassian; Giovanni Stevanin; Karla P Figueroa; John P A Bannister; Dagmar Nolte; Allan F Mock; Virgilio Gerald H Evidente; Dominic B Fee; Ulrich Müller; Alexandra Dürr; Alexis Brice; Diane M Papazian; Stef pulst
Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes.
M F Waters; Dominic B Fee; Karla P Figueroa; Dagmar Nolte; Ulrich Müller; Joel Advincula; Hilary Coon; Virgilio Gerald H Evidente; Stef pulst
An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?
Virgilio Gerald H Evidente; Dagmar Nolte; Stephan Niemann; Joel Advincula; Mezzanie C Mayo; Filipinas F Natividad; Ulrich Müller
Phenotypic and molecular analyses of X-linked dystonia-parkinsonism ("lubag") in women.

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All Publications

2006: Michael F Waters; Natali A Minassian; Giovanni Stevanin; Karla P Figueroa; John P A Bannister; Dagmar Nolte; Allan F Mock; Virgilio Gerald H Evidente; Dominic B Fee; Ulrich Müller; Alexandra Dürr; Alexis Brice; Diane M Papazian; Stef pulst
Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes.
Nature genetics 2006;38(4):447-51.
2005: M F Waters; Dominic B Fee; Karla P Figueroa; Dagmar Nolte; Ulrich Müller; Joel Advincula; Hilary Coon; Virgilio Gerald H Evidente; Stef pulst
An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?
Neurology 2005;65(7):1111-3.
2004: Virgilio Gerald H Evidente; Dagmar Nolte; Stephan Niemann; Joel Advincula; Mezzanie C Mayo; Filipinas F Natividad; Ulrich Müller
Phenotypic and molecular analyses of X-linked dystonia-parkinsonism ("lubag") in women.
Archives of neurology 2004;61(12):1956-9.

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