Splice-Site Mutations: A Novel Genetic Mechanism of Crigler-Najjar Syndrome Type 1-Reference-Cited by-同舟云学术

Splice-Site Mutations: A Novel Genetic Mechanism of Crigler-Najjar Syndrome Type 1

Published:1998-03 Issue:3 Volume:62 Page:585-592
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Gantla Shailaja,Bakker Conny T.M.,Deocharan Bishram,Thummala Narsing R.,Zweiner Jeffry,Sinaasappel Maarten,Roy Chowdhury Jayanta,Bosma Piter J.,Roy Chowdhury Namita

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference26 articles.

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3. Mechanisms of inherited deficiencies of multiple UDP-glucuronosyltransferase isoforms in two patients with Crigler-Najjar syndrome type I;Bosma;FASEB J,1992

4. Bilirubin UDP-glucuronosyltransferase 1 is the only relevant bilirubin glucuronidating isoform in man;Bosma;J Biol Chem,1994

5. Single-step method of RNA isolation by acid guanidium thiocyanate-phenol-chloroform extraction;Chomczynski;Anal Biochem,1987

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