ArticleActa neurologica Belgica2019
A new NBIA patient from Turkey with homozygous C19ORF12 mutation.
Çiğdem Seher Kasapkara et al.PubMed ↗Full text ↗Publisher ↗
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ArticleActa neurologica Belgica2019
Çiğdem Seher Kasapkara et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.