Biallelic Mutations in NBAS Cause Recurrent Acute Liver Failure with Onset in Infancy-Reference-Cited by-同舟云学术

Biallelic Mutations in NBAS Cause Recurrent Acute Liver Failure with Onset in Infancy

Published:2015-07 Issue:1 Volume:97 Page:163-169
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Haack Tobias B.,Staufner Christian,Köpke Marlies G.,Straub Beate K.,Kölker Stefan,Thiel Christian,Freisinger Peter,Baric Ivo,McKiernan Patrick J.,Dikow Nicola,Harting Inga,Beisse Flemming,Burgard Peter,Kotzaeridou Urania,Kühr Joachim,Himbert Urban,Taylor Robert W.,Distelmaier Felix,Vockley Jerry,Ghaloul-Gonzalez Lina,Zschocke Johannes,Kremer Laura S.,Graf Elisabeth,Schwarzmayr Thomas,Bader Daniel M.,Gagneur Julien,Wieland Thomas,Terrile Caterina,Strom Tim M.,Meitinger Thomas,Hoffmann Georg F.,Prokisch Holger

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference19 articles.

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3. Long-term follow-up after recurrence of primary biliary cirrhosis after liver transplantation in 100 patients;Jacob;Clin. Transplant.,2006

4. A defect in the transport of long-chain fatty acids associated with acute liver failure;Odaib;N. Engl. J. Med.,1998

5. Dihydrolipoamide dehydrogenase deficiency: a still overlooked cause of recurrent acute liver failure and Reye-like syndrome;Brassier;Mol. Genet. Metab.,2013

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