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Your search keyword '"Soto‐Ortolaza, Alexandra I."' showing total 8 results

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8 results on '"Soto‐Ortolaza, Alexandra I."'

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1. Study of LRRK2 variation in tauopathy: Progressive supranuclear palsy and corticobasal degeneration

2. MAPT haplotype H1G is associated with increased risk of dementia with Lewy bodies

3. LRRK2 Haplotype-Sharing Analysis in Parkinson's Disease Reveals a Novel p.S1761R Mutation

4. LRRK2 haplotype‐sharing analysis in Parkinson's disease reveals a novel p.S1761R mutation

5. Genetic variants of α-synuclein are not associated with essential tremor

6. Comprehensive sequencing of the LRRK2 gene in patients with familial Parkinson's disease from North Africa

7. Novel pathogenic LRRK2 p.Asn1437His substitution in familial Parkinson's disease

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