Neuropathological Findings in a Case of Parkinsonism and Developmental Delay Associated with a Monoallelic Variant in PLXNA1

O’Shea, S. A., Hickman, R. A., Cortes, E., Vonsattel, J. P., Fahn, S., Okur, V., Alcalay, R. N., & Chung, W. K. (2021). Neuropathological Findings in a Case of Parkinsonism and Developmental Delay Associated with a Monoallelic Variant in PLXNA1. Movement Disorders, 36(11), 2681–2687. Portico. https://doi.org/10.1002/mds.28756
Authors:
Sarah A. O'Shea
Richard A. Hickman
Etty Cortes
Jean Paul Vonsattel
Stanley Fahn
Volkan Okur
Roy N. Alcalay
Wendy K. Chung
Affiliated Authors:
Sarah A. O'Shea
Richard A. Hickman
Etty Cortes
Jean Paul Vonsattel
Stanley Fahn
Volkan Okur
Roy N. Alcalay
Wendy K. Chung
Columbia Affiliation:
Author Keywords:
developmental delay
genetics
parkinsonism
semaphorins
elink
Publication Type:
Article
Unique ID:
10.1002/mds.28756
PMID:
34415653
DOI:
10.1002/mds.28756
Journal:
Movement Disorders
Publication Date:
Data Source:
Scopus
Source Link:
View Scopus Record

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