ArticleHuman genome variation2021
Hyperprolinemia type I caused by homozygous p.T466M mutation in PRODH.
Rina Hama et al.PubMed ↗Full text ↗Publisher ↗
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ArticleHuman genome variation2021
Rina Hama et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.