De la mutación al fenotipo; variabilidad clínica en la enfermedad de Lesch-Nyhan. El papel de la epigenética
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference24 articles.
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Cited by 3 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. Novel mutation in the human HPRT1 gene and the Lesch-Nyhan disease;Nucleosides, Nucleotides and Nucleic Acids;2017-11-02
2. Human HPRT1 gene and the Lesch–Nyhan disease: Substitution of alanine for glycine and inversely in the HGprt enzyme protein;Nucleosides, Nucleotides and Nucleic Acids;2017-01-03
3. The Use of Perinatal 6-Hydroxydopamine to Produce a Rodent Model of Lesch–Nyhan Disease;Neurotoxin Modeling of Brain Disorders—Life-long Outcomes in Behavioral Teratology;2016
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