about
Large-Scale Functional RNAi Screen in C. elegans Identifies TGF-β and Notch Signaling Pathways as Modifiers of CACNA1A.Alteration of ornithine metabolism leads to dominant and recessive hereditary spastic paraplegiaGenomic mechanisms underlying PARK2 large deletions identified in a cohort of patients with PD.Massive sequencing of 70 genes reveals a myriad of missing genes or mechanisms to be uncovered in hereditary spastic paraplegias.Rare Neurodegenerative Diseases: Clinical and Genetic Update.
P50
description
onderzoeker
@nl
researcher ORCID ID = 0000-0003-2543-0376
@en
name
Sara Morais
@ast
Sara Morais
@en
Sara Morais
@es
Sara Morais
@nl
type
label
Sara Morais
@ast
Sara Morais
@en
Sara Morais
@es
Sara Morais
@nl
prefLabel
Sara Morais
@ast
Sara Morais
@en
Sara Morais
@es
Sara Morais
@nl
P106
P1153
56800164700
P21
P31
P496
0000-0003-2543-0376