Heterogeneous Phenotype in a Family With Compound Heterozygous Parkin Gene Mutations-Reference-Cited by-同舟云学术

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Heterogeneous Phenotype in a Family With Compound Heterozygous Parkin Gene Mutations

Published:2006-02-01 Issue:2 Volume:63 Page:273
ISSN:0003-9942
Container-title:Archives of Neurology
language:en
Short-container-title:Arch Neurol

Author:

Deng Hao,Le Wei-Dong,Hunter Christine B.,Ondo William G.,Guo Yi,Xie Wen-Jie,Jankovic Joseph

Publisher

American Medical Association (AMA)

Subject

Clinical Neurology,Arts and Humanities (miscellaneous)

Cited by 42 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. Early Onset Parkinson’s Disease and It’s Genetic Consequences;OSMANGAZİ JOURNAL OF MEDICINE;2024-02-13

2. Two Different PRKN Compound Heterozygous Variants Combinations in the Same Family;Movement Disorders Clinical Practice;2023-03-20

3. Genomic, transcriptomic, and metabolomic profiles of hiPSC-derived dopamine neurons from clinically discordant brothers with identical PRKN deletions;npj Parkinson's Disease;2022-06-29

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

5. Role of Genes and Treatments for Parkinson’s Disease;The Open Biology Journal;2020-10-15

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