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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Bibliografske podrobnosti
Glavni avtor: Faergeman, S
Drugi avtorji: Fugger, L
Format: Thesis
Jezik:English
Izdano: 2018