A branch site mutation leading to aberrant splicing of the human tyrosine hydroxylase gene in a child with a severe extrapyramidal movement disorder-Reference-Cited by-同舟云学术

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A branch site mutation leading to aberrant splicing of the human tyrosine hydroxylase gene in a child with a severe extrapyramidal movement disorder

Published:2000-09 Issue:5 Volume:64 Page:375-382
ISSN:0003-4800
Container-title:Annals of Human Genetics
language:en
Short-container-title:Ann Human Genet

Author:

JANSSEN R. J. R. J.,WEVERS R. A.,HAUSSLER M.,LUYTEN J. A. F. M.,STEENBERGEN-SPANJERS G. C. H.,HOFFMANN G. F.,NAGATSU T.,HEUVEL L. P. W. J.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1469-1809.2000.6450375.x/fullpdf

Cited by 44 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. Catecholamines and Parkinson’s disease: tyrosine hydroxylase (TH) over tetrahydrobiopterin (BH4) and GTP cyclohydrolase I (GCH1) to cytokines, neuromelanin, and gene therapy: a historical overview;Journal of Neural Transmission;2023-08-28

2. Dopa-Responsive Dystonia and Related Disorders;Movement Disorder Emergencies;2021-10-03

3. Genetic polymorphisms in SCN2A are not associated with epilepsy risk and AEDs response: evidence from a meta-analysis;Neurological Sciences;2021-04-29

4. Dystonia;Principles and Practice of Movement Disorders;2021

5. Human tyrosine hydroxylase in Parkinson’s disease and in related disorders;Journal of Neural Transmission;2018-07-11

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