MovDisordV3, Main, Exploration, bibRecord, 000751

The G2019S LRRK2 mutation: another morbid burden for Ashkenazi Jews may provide new insights on sporadic Parkinson's disease.

Identifieur interne : 000751 ( Main/Exploration ); précédent : 000750; suivant : 000752

The G2019S LRRK2 mutation: another morbid burden for Ashkenazi Jews may provide new insights on sporadic Parkinson's disease.

Auteurs : Eldad Melamed [Israël]

Source :

Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2013.

RBID : pubmed:24307480

English descriptors

KwdEn :
- Female, Glycine (genetics), Humans, Male, Mutation (genetics), Parkinson Disease (genetics), Protein-Serine-Threonine Kinases (genetics), Serine (genetics).
MESH :
- chemical , genetics : Glycine, Protein-Serine-Threonine Kinases, Serine.
- genetics : Mutation, Parkinson Disease.
- Female, Humans, Male.

DOI: 10.1002/mds.25728
PubMed: 24307480

Affiliations:

Israël

Le document en format XML

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<affiliation wicri:level="1"><nlm:affiliation>Neurology, Tel Aviv University, Tel Aviv, Israel.</nlm:affiliation>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
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Movement Disorders (revue)

The G2019S LRRK2 mutation: another morbid burden for Ashkenazi Jews may provide new insights on sporadic Parkinson's disease.

The G2019S LRRK2 mutation: another morbid burden for Ashkenazi Jews may provide new insights on sporadic Parkinson's disease.

Source :

English descriptors

Links toward previous steps (curation, corpus...)

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki

	Movement Disorders (revue)
	Attention, ce site est en cours de développement ! Attention, site généré par des moyens informatiques à partir de corpus bruts. Les informations ne sont donc pas validées.