The functional analysis of rare genetic variants in a familial neurodegenerative spectrum disorder

<p>Whole genome sequencing can enable an unbiased approach to the diagnosis and to the understanding of genetic aetiology of neurodegenerative diseases, which are a clinically and genetically heterogeneous group of disorders. Two brothers, originally diagnosed with primary progressive multipl...

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Detalles Bibliográficos
Autor principal: Faergeman, S
Otros Autores: Fugger, L
Formato: Tesis
Lenguaje:English
Publicado: 2018