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...

Deskribapen osoa

Xehetasun bibliografikoak
Egile nagusia: Faergeman, S
Beste egile batzuk: Fugger, L
Formatua: Thesis
Hizkuntza:English
Argitaratua: 2018