Author:
Ferreira Gabriela K.,Jeremias Isabela C.,Scaini Giselli,Carvalho-Silva Milena,Gomes Lara M.,Furlanetto Camila B.,Morais Meline O.,Schuck Patrícia F.,Ferreira Gustavo C.,Streck Emilio L.
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,General Medicine,Biochemistry
Reference35 articles.
1. Mitchell GA, Grompe M, Lambert M, Tanguay RM (2001) Hypertyrosinemia. In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds) The metabolic and molecular bases of inherited disease. McGraw-Hill, New York, pp 1977–1982
2. Held PK (2006) Disorders of tyrosine catabolism. Mol Genet Metab 88:103–106
3. Paige DG, Clayton P, Bowron A, Harper JL (1992) Richner–Hanhart syndrome (oculocutaneous tyrosinaemia, tyrosinaemia type II). J R Soc Med 85:759–760
4. Chakrapani A, Holme E (2006) Disorders of tyrosine metabolism. In: Fernandes J, Saudubray JM, Van den Berghe G, Walter JM (eds) Inborn metabolic diseases. diagnosis and treatment, 4th edn. Springer, Würzburg, pp 233–243
5. Madan V, Gupta U (2006) Tyrosinaemia type II with diffuse plantar keratoderma and self-mutilation. Clin Exp Dermatol 31:54–56
Cited by
11 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