Author:
Hanisch F.,Joshi P.,Zierz S.
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Reference17 articles.
1. Fishbein WN, Armbrustmacher VW, Griffin JL (1980) Myoadenylate deaminase deficiency: a new disease of muscle. Science 200:545–548
2. Fishbein WN (1986) Myoadenylate deaminase deficiency: primary and secondary types. Toxicol Ind Health 2:105–118
3. Morisaki T, Gross M, Morisaki H, Pongratz D, Zöllner N, Holmes EW (1992) Molecular basis of AMP deaminase deficiency in skeletal muscle. Proc Natl Acad Sci USA 15:6457–6461
4. Verzijl HT, van Engelen BG, Luyten JA (1998) Genetic characterization of myoadenylate deaminase deficiency. Ann Neurol 44:140–143
5. Fischer S, Drenckhahn C, Wolf C et al. (2005) Clinical significance and neuropathology of primary MADD in C34-T and G468-T mutations of the AMPD1 gene. Clin Neuropathol 24:77–85
Cited by
26 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