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Autosomal dominant myofibrillar myopathy with arrhythmogenic right ventricular cardiomyopathy linked to chromosome 10q

Author
MELBERG, A1 ; OLDFORS, A2 ; DAHL, N5 ; BLOMSTRÖM-LUNDQVIST, C3 ; STALBERG, E4 ; CARLSSON, B5 ; LARSSON, E6 ; LIDELL, C3 ; EEG-OLOFSSON, K. E4 ; WIKSTRÖM, G3 ; HENRIKSSON, K. G7
[1] Department of Neuroscience, Neurology, Department of Genetics and Pathology, Uppsala University Hospital, Uppsala, Sweden
[2] Department of Pathology, Gothenburg University, Sahlgrenska Hospital, Göteborg, Sweden
[3] Department of Cardiology, Uppsala University Hospital, Uppsala, Sweden
[4] Department of Clinical Neurophysiology, Department of Genetics and Pathology, Uppsala University Hospital, Uppsala, Sweden
[5] Clinical Genetics, Uppsala University Hospital, Uppsala, Sweden
[6] Pathology, Uppsala University Hospital, Uppsala, Sweden
[7] Neuromuscular Unit, Linköping University Hospital, Linköping, Sweden
Source

Annals of neurology. 1999, Vol 46, Num 5, pp 684-692 ; ref : 42 ref

CODEN
ANNED3
ISSN
0364-5134
Scientific domain
Neurology
Publisher
Willey-Liss, Hoboken
Publication country
United Kingdom
Document type
Article
Language
English
Keyword (fr)
Anatomopathologie Association morbide Cardiomyopathie Chromosome C10 Etude familiale Exploration Homme Liaison génétique Myopathie myotubulaire Trouble rythme cardiaque Ventricule droit Appareil circulatoire pathologie Cardiopathie Génétique Maladie congénitale Muscle strié pathologie Myocarde pathologie
Keyword (en)
Pathology Concomitant disease Cardiomyopathy Chromosome C10 Family study Exploration Human Linkage Myotubular myopathy Arrhythmia Right ventricle Cardiovascular disease Heart disease Genetics Congenital disease Striated muscle disease Myocardial disease
Keyword (es)
Anatomía patológica Asociación morbosa Cardiomiopatía Cromosoma C10 Estudio familiar Exploración Hombre Ligamiento genético Miopatía miotubular Arritmia Ventrículo derecho Aparato circulatorio patología Cardiopatía Genética Enfermedad congénita Músculo estriado patología Miocardio patología
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17H Diseases of striated muscles. Neuromuscular diseases

Discipline
Neurology
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
1183470

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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