Clinical and genetic studies on familial parkinsonism: the first report on a parkin gene mutation in a Taiwanese family.
Identifieur interne : 006A90 ( Main/Merge ); précédent : 006A89; suivant : 006A91Clinical and genetic studies on familial parkinsonism: the first report on a parkin gene mutation in a Taiwanese family.
Auteurs : C S Lu [Taïwan] ; J C Wu ; C H Tsai ; R S Chen ; Y H Chou ; N. Hattori ; H. Yoshino ; Y. MizunoSource :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2001.
Descripteurs français
- Wicri :
- geographic : Taïwan.
English descriptors
- KwdEn :
- Adolescent, Adult, Aged, Chromosomes, Human, Pair 6 (genetics), Dopamine (metabolism), Exons, Female, Gene Deletion, Humans, Ligases, Male, Middle Aged, Parkinsonian Disorders (diagnosis), Parkinsonian Disorders (genetics), Pedigree, Point Mutation (genetics), Proteins (genetics), Substantia Nigra (metabolism), Taiwan, Ubiquitin-Protein Ligases.
- MESH :
- chemical , genetics : Proteins.
- chemical , metabolism : Dopamine.
- geographic : Taiwan, Ubiquitin-Protein Ligases.
- diagnosis : Parkinsonian Disorders.
- genetics : Chromosomes, Human, Pair 6, Parkinsonian Disorders, Point Mutation.
- metabolism : Substantia Nigra.
- Adolescent, Adult, Aged, Exons, Female, Gene Deletion, Humans, Ligases, Male, Middle Aged, Pedigree.
PubMed: 11215581
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pubmed:11215581Le document en format XML
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Hattori</name></author><author><name sortKey="Yoshino, H" sort="Yoshino, H" uniqKey="Yoshino H" first="H" last="Yoshino">H. Yoshino</name></author><author><name sortKey="Mizuno, Y" sort="Mizuno, Y" uniqKey="Mizuno Y" first="Y" last="Mizuno">Y. 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Hattori</name></author><author><name sortKey="Yoshino, H" sort="Yoshino, H" uniqKey="Yoshino H" first="H" last="Yoshino">H. Yoshino</name></author><author><name sortKey="Mizuno, Y" sort="Mizuno, Y" uniqKey="Mizuno Y" first="Y" last="Mizuno">Y. Mizuno</name></author></analytic><series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title><idno type="ISSN">0885-3185</idno><imprint><date when="2001" type="published">2001</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adolescent</term><term>Adult</term><term>Aged</term><term>Chromosomes, Human, Pair 6 (genetics)</term><term>Dopamine (metabolism)</term><term>Exons</term><term>Female</term><term>Gene Deletion</term><term>Humans</term><term>Ligases</term><term>Male</term><term>Middle Aged</term><term>Parkinsonian Disorders (diagnosis)</term><term>Parkinsonian Disorders (genetics)</term><term>Pedigree</term><term>Point Mutation (genetics)</term><term>Proteins (genetics)</term><term>Substantia Nigra (metabolism)</term><term>Taiwan</term><term>Ubiquitin-Protein Ligases</term></keywords><keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Proteins</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Dopamine</term></keywords><keywords scheme="MESH" type="geographic" xml:lang="en"><term>Taiwan</term><term>Ubiquitin-Protein Ligases</term></keywords><keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Parkinsonian Disorders</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Chromosomes, Human, Pair 6</term><term>Parkinsonian Disorders</term><term>Point Mutation</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Substantia Nigra</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Adolescent</term><term>Adult</term><term>Aged</term><term>Exons</term><term>Female</term><term>Gene Deletion</term><term>Humans</term><term>Ligases</term><term>Male</term><term>Middle Aged</term><term>Pedigree</term></keywords><keywords scheme="Wicri" type="geographic" xml:lang="fr"><term>Taïwan</term></keywords></textClass></profileDesc></teiHeader></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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