A rare novel deletion of the tyrosine hydroxylase gene in Parkinson disease-Reference-Cited by-同舟云学术

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A rare novel deletion of the tyrosine hydroxylase gene in Parkinson disease

Published:2010-08-31 Issue:10 Volume:31 Page:E1767-E1771
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Bademci Güney,Edwards Todd L.,Torres Andre L.,Scott William K.,Züchner Stephan,Martin Eden R.,Vance Jeffery M.,Wang Liyong

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Cited by 30 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

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5. Tyrosine hydroxylase deficiency—Clinical insights and a novel deletion in TH gene in an Indian patient;JIMD Reports;2020-02-29

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