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Homozygous 1311G > A PINK1 mutation in a patient with Parkinson disease, psychiatric disorder, and apparently dominant transmission

VALENTE, ENZA MARIA;
2005-01-01
2005
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.
MOVEMENT DISORDERS
WOS:000227212400476
Comitato scientifico
Inglese
9th International Congress of Parkinsons Disease and Movement Disorders
MAR 05-08, 2005
New Orleans, LA
Internazionale
20
S140
S140
1
WILEY-LISS, DIV JOHN WILEY & SONS INC
111 RIVER ST, HOBOKEN, NJ 07030 USA
STATI UNITI D'AMERICA
no
6
info:eu-repo/semantics/conferenceObject
none
274
4 Contributo in Atti di Convegno (Proceeding)::4.2 Abstract in Atti di convegno
Criscuolo, C; Volpe, G; De Rosa, A; Filla, A; Valente, ENZA MARIA; De Michele, G.
4.2 Abstract in Atti di convegno
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/1180728
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