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3. A homozygous mutation of C12orf65 causes spastic paraplegia with optic atrophy and neuropathy (SPG55). Issue 12 (27th November 2012)

5. Application of multiple γ-ray detection to long-lived radioactive nuclide determination in environmental samples. Issue 6 (2nd June 2020)

7. Atypical parkinsonism caused by Pro105Leu mutation of prion protein: A broad clinical spectrum. (February 2016)

8. Autosomal-recessive complicated spastic paraplegia with a novel lysosomal trafficking regulator gene mutation. Issue 9 (12th February 2014)

9. Burden of rare variants in causative genes for amyotrophic lateral sclerosis (ALS) accelerates age at onset of ALS. Issue 5 (24th October 2018)