Literature DB >> 6143470

Deficiency of tyrosine hydroxylase or tryptophan hydroxylase: a possible cause of two hypothetical metabolic diseases.

K Bartholomé.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1983        PMID： 6143470     DOI： 10.1111/j.1651-2227.1983.tb09842.x

Source DB:  PubMed          Journal:  Acta Paediatr Scand        ISSN： 0001-656X


× No keyword cloud information.
  2 in total

Review 1.  Tyrosine hydroxylase and Parkinson's disease.

Authors:  J Haavik; K Toska
Journal:  Mol Neurobiol       Date:  1998-06       Impact factor: 5.590

2.  A point mutation in the tyrosine hydroxylase gene associated with Segawa's syndrome.

Authors:  B Lüdecke; B Dworniczak; K Bartholomé
Journal:  Hum Genet       Date:  1995-01       Impact factor: 4.132
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.