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...

Πλήρης περιγραφή

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριος συγγραφέας: Faergeman, S
Άλλοι συγγραφείς: Fugger, L
Μορφή: Thesis
Γλώσσα:English
Έκδοση: 2018