ArticleJournal of human genetics2023
Correction: A novel homozygous CHMP1A variant arising from segmental uniparental disomy causes pontocerebellar hypoplasia type 8.
Masamune Sakamoto et al.PubMed ↗Publisher ↗
No numbers read from the abstract.
ArticleJournal of human genetics2023
Masamune Sakamoto et al.PubMed ↗Publisher ↗
No numbers read from the abstract.