Defining the Epsilon-Sarcoglycan (SGCE) Gene Phenotypic Signature in Myoclonus-Dystonia: A Reappraisal of Genetic Testing Criteria

SGCE mutations cause psychiatric disorders: clinical and genetic characterization

(2013) Kathryn J. Peall et al.   BRAIN

Cognition and psychopathology in myoclonus-dystonia

(2012) Mirjam J van Tricht et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

A novel mutation of the SGCE-gene in a German family with myoclonus-dystonia syndrome

(2011) Christian Johannes Hartmann et al.   JOURNAL OF NEUROLOGY

Psychiatric disorders, myoclonus dystonia, and the epsilon-sarcoglycan gene: A systematic review

(2011) Kathryn J. Peall et al.   MOVEMENT DISORDERS

Familial 7q21.3 microdeletion involving epsilon-sarcoglycan causing myoclonus dystonia, cognitive impairment, and psychosis

(2011) Russell C. Dale et al.   MOVEMENT DISORDERS

Expanding the phenomenology of benign hereditary chorea: Evolution from chorea to myoclonus and dystonia

(2011) Melissa J. Armstrong et al.   MOVEMENT DISORDERS

Myoclonus dystonia plus syndrome due to a novel 7q21 microdeletion

(2010) Pascale Saugier-Veber et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Myoclonus-dystonia: An update

(2009) Kiyoka Kinugawa et al.   MOVEMENT DISORDERS

Pediatric writer's cramp in myoclonus-dystonia: Maternal imprinting hides positive family history

(2008) M.C.F. Gerrits et al.   EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY

Myoclonus-dystonia: significance of largeSGCEdeletions

(2008) A. Grünewald et al.   HUMAN MUTATION

Cryptic 7q21 and 9p23 deletions in a patient with apparently balanced de novo reciprocal translocation t(7;9)(q21;p23) associated with a dystonia-plus syndrome: paternal deletion of the epsilon-sarcoglycan (SGCE) gene

(2008) C. Bonnet et al.   JOURNAL OF HUMAN GENETICS

Myoclonus-dystonia: clinical and genetic evaluation of a large cohort

(2008) K Ritz et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Phenotypic spectrum and sex effects in eleven myoclonus-dystonia families with ɛ-sarcoglycan mutations

(2008) Deborah Raymond et al.   MOVEMENT DISORDERS

Unusual familial presentation of epsilon-sarcoglycan gene mutation with falls and writer's cramp

(2008) Vasiliki Koukouni et al.   MOVEMENT DISORDERS

Myoclonus–dystonia syndrome: Clinical presentation, disease course, and genetic features in 11 families

(2007) Nardo Nardocci et al.   MOVEMENT DISORDERS

Large deletions account for an increasing number of mutations inSGCE

(2007) Fabin Han et al.   MOVEMENT DISORDERS