ArticleJournal of human genetics2020
IDDCA syndrome in a Chinese infant due to GNB5 biallelic mutations.
Mingxing Tang et al.PubMed ↗Publisher ↗
No numbers read from the abstract.
4 papers cite it
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ArticleJournal of human genetics2020
Mingxing Tang et al.PubMed ↗Publisher ↗
No numbers read from the abstract.