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Coding defect and a TATA box mutation at the bilirubin UDP-glucuronosyltransferase gene cause Crigler-Najjar type I disease

✍ Scribed by M. Ciotti; F. Chen; F.F. Rubaltelli; I.S. Owens

No coin nor oath required. For personal study only.

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Sequence of exons and the flanking regio

✍ Piter J. Bosma; Namita Roy Chowdhury; Bart G. Goldhoorn; Martin H. Hofker; Ronal 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 814 KB

Crigler-Najjar syndrome, type I is a heterogeneous