7 results on '"Gana Weisz, Mali"'
Search Results
2. Contribution of Rare Homozygous Variants in ALS in a Homogenous Population (P4.441)
3. Application of the Movement Disorder Society Prodromal Criteria in healthy G2019S-LRRK2 carriers (S3.002)
4. OPTN691_692insAG is a founder mutation causing recessive ALS and increased risk in heterozygotes
5. OPTN 691_692insAG is a founder mutation causing recessive ALS and increased risk in heterozygotes.
6. Differential effects of severe vs mild GBA mutations on Parkinson disease.
7. The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.