@article{12578aa1f76748ed9d59b1a3c49c671b,
title = "Phenotypic variability of PINK1 expression: 12 Years' clinical follow-up of two Italian families",
abstract = "Mutations in the PINK1 gene are the second most frequent cause of autosomal recessive early-onset parkinsonism.",
keywords = "PINK1, Parkinson disease, autosomal recessive early-onset parkinsonism, heterozygotes, nonmotor signs, PINK1, Parkinson disease, autosomal recessive early-onset parkinsonism, heterozygotes, nonmotor signs",
author = "Lucia Ricciardi and Simona Petrucci and Arianna Guidubaldi and Tamara Ialongo and Laura Serra and Alessandro Ferraris and Barbara Span{\`o} and Marco Bozzali and Valente, {Enza Maria} and Bentivoglio, {Anna Rita}",
year = "2014",
doi = "10.1002/mds.25994",
language = "English",
volume = "29",
pages = "1561--1566",
journal = "Movement Disorders",
issn = "0885-3185",
publisher = "-WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, USA, NJ, 07030 -Lippincott, Williams & Wilkins:530 Walnut Street:Philadelphia, PA 19106:(800)638-3030, (301)223-2300, EMAIL: orders@lww.com, INTERNET: http://www.lww.com, Fax: (301)223-2320, (301)223-2320",
}