Predictive sensitivity and concordance of machine-learning tools for diagnosing DFNA9 in a large series of p.Pro51Ser variant carriers in the COCH-gene

Source
Otology and neurotology - ISSN 1531-7129-42:5 (2021) p. 671-677
Author(s)

Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson's disease

Source
Acta neuropathologica communications - ISSN 2051-5960-9:1 (2021) p.
Author(s)