Associated Papers
A Novel Homozygous Variant of SETX Causes Ataxia with Oculomotor Apraxia Type 2.
Tariq H et al.
Journal of Clinical Neurology (seoul, Korea), 2018
30198223 (PubMed )
Supplement: jcn-14-498-s001.xls › homo_0.01_filter
Can unknown predisposition in familial breast cancer be family-specific?
Lynch H et al.
The Breast Journal, 0
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