Genomic deletions upstream of lamin B1 lead to atypical autosomal dominant leukodystrophy (vol 5, e305, 2019)

Journal article

Open access

Peer reviewed

B. Nmezi, E. Giorgio, R. Raininko, A. Lehman, M. Spielmann, M. K. Koenig, R. Adejumo, M. Knight, R. Gavrilova, M. Alturkustani, …

Neurology. Genetics, Vol.5(5), p.e362

01/10/2019

PMCID: PMC6807656

PMID: 31742230

Abstract

Clinical Neurology

Genetics & Heredity

Life Sciences & Biomedicine

Neurosciences & Neurology

Science & Technology

url

https://doi.org/10.1212/NXG.0000000000000362View

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Title: Genomic deletions upstream of lamin B1 lead to atypical autosomal dominant leukodystrophy (vol 5, e305, 2019)
Creators - without role: B. Nmezi
E. Giorgio
R. Raininko
A. Lehman
M. Spielmann
M. K. Koenig
R. Adejumo
M. Knight
R. Gavrilova
M. Alturkustani
M. Sharma
R. Hammond
W. A. Gahl
C. Toro
A. Brusco
Q. S. Padiath
Publication Details: Neurology. Genetics, Vol.5(5), p.e362
Publisher: Lippincott Williams & Wilkins
Number of pages: 1
Grant note: R01NS095884 / NIH; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA
Identifiers: 9936517808331
Academic Unit: King Abdulaziz University
Language: English
Resource Type: Journal article