✦ LIBER ✦

Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1

✍ Scribed by Valente, E. M.

Book ID: 119942517
Publisher: American Association for the Advancement of Science
Year: 2004
Tongue: English
Weight: 250 KB
Volume: 304
Category: Article
ISSN: 0036-8075
DOI: 10.1126/science.1096284

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

PINK1 mutations in sporadic early-onset

PINK1 mutations in sporadic early-onset Parkinson's disease

✍ Eng-King Tan; Kenneth Yew; Eva Chua; K. Puvan; Hui Shen; Esther Lee; Kim-Yoong P 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 347 KB 👁 1 views

## Abstract Pathogenic __PINK1__ mutations have been described in PARK6‐linked Parkinson's disease (PD) patients of Asian origin. However, data on the frequency of __PINK1__ mutations in sporadic early‐onset Parkinson's disease (EOPD) Asian patients are lacking. The objectives of this study were to

Homozygous PINK1 C-terminus mutation cau

Homozygous PINK1 C-terminus mutation causing early-onset parkinsonism

✍ Christan F. Rohé; Pasquale Montagna; Guido Breedveld; Pietro Cortelli; Ben A. Oo 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 508 KB

PINK1 mutation in Taiwanese early-onset

PINK1 mutation in Taiwanese early-onset parkinsonism

✍ Yi-Hsin Weng; Yah-Huei Wu Chou; Wen-Shiang Wu; Kun-Ju Lin; Hsiu-Chen Chang; Tzu- 📂 Article 📅 2007 🏛 Springer 🌐 English ⚖ 297 KB

Novel PINK1 mutations in early-onset par

Novel PINK1 mutations in early-onset parkinsonism

✍ Yasuko Hatano; Yuanzhe Li; Kenichi Sato; Shuichi Asakawa; Yasuhiro Yamamura; Hir 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 412 KB 👁 1 views

Late onset sporadic Parkinson's disease

Late onset sporadic Parkinson's disease caused by PINK1 mutations: Clinical and functional study

✍ Vania Gelmetti; Alessandro Ferraris; Livia Brusa; Francesca Romano; Federica Lom 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 153 KB 👁 1 views

## Abstract Homozygous or compound heterozygous mutations in the __PINK1__ gene represent the second most frequent cause of autosomal recessive parkinsonism after __Parkin__. The phenotype differs from idiopathic Parkinson's disease for earlier onset, slower disease progression, and better response

PINK1 mutations in a Brazilian cohort of

PINK1 mutations in a Brazilian cohort of early-onset Parkinson's disease patients

✍ Clecio Godeiro-Junior; Patricia M. de Carvalho-Aguiar; Andre C. Felício; Orlando 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 218 KB 👁 1 views

## Abstract Data on the frequency of __PINK1__ mutations in Brazilian patients with early‐onset Parkinson's disease (EOPD) are lacking. The aim of this report was to investigate mutations of the __PINK1__ gene in a cohort of Brazilian patients with EOPD. Sixty consecutive familial or sporadic EOPD