His1069Gln and six novel Wilson disease mutations: analysis of relevance for early diagnosis and phenotype-Reference-Cited by-同舟云学术

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His1069Gln and six novel Wilson disease mutations: analysis of relevance for early diagnosis and phenotype

Published:1998-11 Issue:6 Volume:6 Page:616-623
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Ha-Hao Duc,Hefter Harald,Stremmel Wolfgang,Castañeda-Guillot Carlos,Hernández Ana Hernández,Cox Diane W,Auburger Georg

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/5200237.pdf

Cited by 40 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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3. In Vivo Exon Replacement in the Mouse Atp7b Gene by the Cas9 System;Human Gene Therapy;2019-09-01

4. Molecular genetic diagnosis of Wilson disease by ARMS-PCR in a Pakistani family;Molecular Biology Reports;2018-11-13

5. Characterization of mutation spectrum and identification of novel mutations in ATP7B gene from a cohort of Wilson disease patients: Functional and therapeutic implications;Human Mutation;2018-09-16

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