Neurological Wilson's disease lethal for the son, asymptomatic in the father.
Identifieur interne : 000893 ( Main/Exploration ); précédent : 000892; suivant : 000894Neurological Wilson's disease lethal for the son, asymptomatic in the father.
Auteurs : Yves Denoyer ; France Woimant ; Muriel Bost ; Gilles Edan ; Sophie DrapierSource :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2013.
English descriptors
- KwdEn :
- Adenosine Triphosphatases (genetics), Adult, Cation Transport Proteins (genetics), Copper (metabolism), Family Health, Fathers, Female, Hepatolenticular Degeneration (genetics), Hepatolenticular Degeneration (pathology), Hepatolenticular Degeneration (physiopathology), Humans, Magnetic Resonance Imaging, Male, Young Adult.
- MESH :
- chemical , genetics : Adenosine Triphosphatases, Cation Transport Proteins.
- chemical , metabolism : Copper.
- genetics : Hepatolenticular Degeneration.
- pathology : Hepatolenticular Degeneration.
- physiopathology : Hepatolenticular Degeneration.
- Adult, Family Health, Fathers, Female, Humans, Magnetic Resonance Imaging, Male, Young Adult.
DOI: 10.1002/mds.25290
PubMed: 23389864
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 000A90
- to stream PubMed, to step Curation: 000A90
- to stream PubMed, to step Checkpoint: 000908
- to stream Ncbi, to step Merge: 003991
- to stream Ncbi, to step Curation: 003991
- to stream Ncbi, to step Checkpoint: 003991
- to stream Main, to step Merge: 000893
- to stream Main, to step Curation: 000893
Le document en format XML
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