Related references
Note: Only part of the references are listed.Milestones in Huntington Disease
Ira Shoulson et al.
MOVEMENT DISORDERS (2011)
Conducting Meta-Analyses in R with the metafor Package
Wolfgang Viechtbauer
JOURNAL OF STATISTICAL SOFTWARE (2010)
Evidence for a predisposing background for CAG expansion leading to HTT mutation in a Chinese population
Mingyi Ma et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2010)
Accurate prevalence and uptake of testing for Huntington's disease
Patrick J. Morrison
LANCET NEUROLOGY (2010)
Nationwide Population-Based Epidemiologic Study of Huntington's Disease in Taiwan
Yen-Yu Chen et al.
NEUROEPIDEMIOLOGY (2010)
Epidemiology of Huntington's disease in Slovenia
B. Peterlin et al.
ACTA NEUROLOGICA SCANDINAVICA (2009)
CAG Expansion in the Huntington Disease Gene Is Associated with a Specific and Targetable Predisposing Haplogroup
Simon C. Warby et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2009)
Incidence of early-onset dementias in Cambridgeshire, United Kingdom
L. Mercy et al.
NEUROLOGY (2008)
The Huntington's disease-like syndromes: what to consider in patients with a negative Huntington's disease gene test
Susanne A. Schneider et al.
NATURE CLINICAL PRACTICE NEUROLOGY (2007)
Incidence and mutation rates of Huntington's disease in Spain: experience of 9 years of direct genetic testing
MA Ramos-Arroyo et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2005)
CAG/CTG repeat expansions at the Huntington's disease-like 2 locus are rare in Huntington's disease patients
G Stevanin et al.
NEUROLOGY (2002)
High incidence rate and absent family histories in one quarter of patients newly diagnosed with Huntington disease in British Columbia
EW Almqvist et al.
CLINICAL GENETICS (2001)
Measurement of mutational flow implies both a high new-mutation rate for Huntington disease and substantial underascertainment of late-onset cases
D Falush et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2001)