ArticleAnnals of neurology2016
Truncating mutations in APP cause a distinct neurological phenotype.
Steven Klein et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
12 papers cite it
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ArticleAnnals of neurology2016
Steven Klein et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.