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You searched for: Author/Creator Mundwiller, Emeline

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1. CIC inactivating mutations identify aggressive subset of 1p19q codeleted gliomas. Issue 3 (27th July 2015)

2. Heterozygous PNPT1 Variants Cause Spinocerebellar Ataxia Type 25. Issue 1 (7th May 2022)

3. Spinocerebellar ataxia type 11 (SCA11) is an uncommon cause of dominant ataxia among French and German kindreds. Issue 11 (28th July 2010)

4. The impact of rare variants in FUS in essential tremor. Issue 5 (28th January 2015)