McLeod syndrome: Five new pedigrees with novel mutations.

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• Overview
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• Research
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• Identity
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• Additional Document Info
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Overview

authors

• Weaver, J
• Niotis, K
• Scharre, D W
• Tuite, P
• Stutz, A
• Westhoff, C M
• Walker, R H
• Sarva, H
• Barone, D
• Bobker, S
• Bushara, K
• Hiller, A
• Makoto Ishii, MD, PhD
• Jankovic, J
• Lakhani, S

publication date

• January 1, 2019

published in

• Parkinsonism & related disorders  Journal

has subject area

• Adult
• Amino Acid Transport Systems, Neutral
• Comorbidity
• Creatine Kinase
• Europe
• Humans
• Male
• Middle Aged
• Mutation
• Neuroacanthocytosis
• Pedigree
• Retrospective Studies
• Sleep Apnea, Obstructive
• Vietnam

Research

Keywords

• McLeod syndrome
• Neuroacanthocytosis
• Obstructive sleep apnea
• hyperCKemia

Identity

Digital Object Identifier (DOI)

• https://doi.org/10.1016/j.parkreldis.2019.04.022

PubMed ID

• 31103486

Additional Document Info

start page

• 293

end page

• 299