Myoadenylate deaminase deficiency caused by alternative splicing due to a novel intronic mutation in the AMPD1 gene-Reference-Cited by-同舟云学术

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Myoadenylate deaminase deficiency caused by alternative splicing due to a novel intronic mutation in the AMPD1 gene

Published:2005-09 Issue:1-2 Volume:86 Page:250-256
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Isackson Paul J.,Bujnicki Heather,Harding Cary O.,Vladutiu Georgirene D.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Cited by 13 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Biochemical and physiological investigations on adenosine 5ʹ monophosphate deaminase from Plasmodium spp .;Molecular Microbiology;2019-07-05

2. Biochemical and physiological investigations on adenosine 5’ monophosphate deaminase from Plasmodium spp.;2018-10-19

3. The Sarcomeric M-Region: A Molecular Command Center for Diverse Cellular Processes;BioMed Research International;2015

4. Confirmación genética del déficit de mioadenilato desaminasa;Revista de Neurología;2014

5. Exertional Rhabdomyolysis;Journal of Clinical Neuromuscular Disease;2012-03

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