Lack of mutation G209A in the alpha-synuclein gene in French patients with familial and sporadic Parkinson's disease.
Identifieur interne : 003F53 ( Main/Exploration ); précédent : 003F52; suivant : 003F54Lack of mutation G209A in the alpha-synuclein gene in French patients with familial and sporadic Parkinson's disease.
Auteurs : G. Lucotte ; G. Mercier ; J C TurpinSource :
- Journal of neurology, neurosurgery, and psychiatry [ 0022-3050 ] ; 1998.
Descripteurs français
- Wicri :
- geographic : France.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : Nerve Tissue Proteins, Phosphoproteins.
- geographic : France, Synucleins, alpha-Synuclein.
- genetics : Parkinson Disease, Point Mutation.
- Adult, Aged, Aged, 80 and over, Female, Humans, Male, Middle Aged, Periodicity.
PubMed: 9854985
Affiliations:
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Le document en format XML
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<author><name sortKey="Turpin, J C" sort="Turpin, J C" uniqKey="Turpin J" first="J C" last="Turpin">J C Turpin</name>
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<author><name sortKey="Mercier, G" sort="Mercier, G" uniqKey="Mercier G" first="G" last="Mercier">G. Mercier</name>
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<series><title level="j">Journal of neurology, neurosurgery, and psychiatry</title>
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<term>Nerve Tissue Proteins (genetics)</term>
<term>Parkinson Disease (genetics)</term>
<term>Periodicity</term>
<term>Phosphoproteins (genetics)</term>
<term>Point Mutation (genetics)</term>
<term>Synucleins</term>
<term>alpha-Synuclein</term>
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<term>Phosphoproteins</term>
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<term>Synucleins</term>
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