Defining the phenotypic signature of SGCE mutations in myoclonus-dystonia patients

VALENTE, ENZA MARIA
2011-01-01

2011
MOVEMENT DISORDERS
Molecular Biology & Genetics considers all aspects of basic and applied genetics, including molecular genetics, prokaryotic and eukaryotic gene expression, mechanisms of mutagenesis, structure, function and regulation of genetic material. Also included are resources concerned with clinical genetics, patterns of inheritance, genetic cause, and screening and treatment of disease. Resources dealing specifically with developmentally regulated gene expression, or with signal transduction pathways that modulate gene expression at the cellular level are excluded and are covered in the Cell and Developmental Biology category.
The Neurology category covers resources concerned with the central and peripheral nervous system including the brain, spinal cord, nerves, and fluids. Coverage includes general and clinical neurology including neurosurgery, neuropsychiatry, neuropsychology, neurophysiology, neuroradiology, neuropediatrics, neuropathology, and neurobiology. Resources on cerebrovascular diseases, movement and spinal disorders, pain, dementia, headache, aphasiology, brain injury, paraplegia, stroke, and acupuncture are also included.
Comitato scientifico
Inglese
15th International Congress of Parkinsons Disease and Movement Disorders
2011
Toronto, Canada
Internazionale
26
S324
S324
1
WILEY-BLACKWELL
Malden
STATI UNITI D'AMERICA
no
8
info:eu-repo/semantics/conferenceObject
none
274
4 Contributo in Atti di Convegno (Proceeding)::4.2 Abstract in Atti di convegno
Carecchio, M.; Bonetti, M.; Magliozzi, M.; Edwards, M. J.; Ferraris, A.; Torrente, I.; Bhatia, K. P.; Valente, ENZA MARIA
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/1177992
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