Pantothenate kinase–associated neurodegeneration: Clinical description of 10 patients and identification of new mutations
Identifieur interne : 001492 ( Main/Curation ); précédent : 001491; suivant : 001493Pantothenate kinase–associated neurodegeneration: Clinical description of 10 patients and identification of new mutations
Auteurs : Salima Assami [Algérie] ; Hamid Azzedine [France] ; Sonia Nouioua [Algérie] ; Emeline Mundwiller [France] ; Soulaiman Mahoui [Algérie] ; Samira Makri ; Meriam Djemai [Algérie] ; Djamel Grid [France] ; Alexis Brice [France] ; Tarik Hamadouche [Algérie] ; Giovanni Stevanin [France] ; Meriem Tazir [Algérie]Source :
- Movement Disorders [ 0885-3185 ] ; 2011-08-01.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Homme.
English descriptors
- KwdEn :
- Adolescent, Child, Child, Preschool, Family Health, Female, Genetic Association Studies (methods), Genetic Predisposition to Disease (genetics), Human, Humans, Male, Mutation, Mutation (genetics), Nervous system diseases, Neurodegenerative Diseases (genetics), Pantothenate kinase, Phosphotransferases (Alcohol Group Acceptor) (genetics), Young Adult.
- MESH :
- chemical , genetics : Phosphotransferases (Alcohol Group Acceptor).
- genetics : Genetic Predisposition to Disease, Mutation, Neurodegenerative Diseases.
- methods : Genetic Association Studies.
- Adolescent, Child, Child, Preschool, Family Health, Female, Humans, Male, Young Adult.
Url:
DOI: 10.1002/mds.23648
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ISTEX:7596CA5942AC4AB830B1B49687E3765301C16072Curation
No country items
Samira Makri<affiliation><wicri:noCountry code="no comma">EHS Ali Ait Idir</wicri:noCountry>
</affiliation>
Le document en format XML
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<series><title level="j">Movement Disorders</title>
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