Paracelsus Medizinische Privatuniversität (PMU)

Forschung & Innovation
Publikationen

A single nucleotide polymorphism in the coding region of PGC-1α is a male-specific modifier of Huntington disease age-at-onset in a large European cohort.

#2014
#BMC NEUROLOGY

PMU Autor*innen
Selma M. Soyal, Wolfgang Patsch

Alle Autor*innen
Patrick Weydt, Selma M. Soyal, G Bernhard Landwehrmeyer, Wolfgang Patsch

Fachzeitschrift
BMC NEUROLOGY

Kurzfassung

Keywords

DEFECTS, SEQUENCE, PATHOGENESIS, SEX-DIFFERENCES, MICE, NEURODEGENERATION, LOCALIZATION, COACTIVATOR, OF-ONSET, GENETIC MODIFIERS