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1. A high‐content drug screening strategy to identify protein level modulators for genetic diseases: A proof‐of‐principle in autosomal dominant leukodystrophy. Issue 1 (8th December 2020)

2. A novel homozygous change of CLCN2 (p.His590Pro) is associated with a subclinical form of leukoencephalopathy with ataxia (LKPAT). Issue 10 (4th May 2017)

6. Docosahexaenoic acid is a beneficial replacement treatment for spinocerebellar ataxia 38. Issue 4 (22nd October 2017)

7. Exome sequencing in children of women with skewed X-inactivation identifies atypical cases and complex phenotypes. (May 2017)