Hereditary spastic paraplegia and extensive leukoencephalopathy: a case report of a unique phenotype associated with a GJB1/Cx32 p.Pro174Ser variant-Reference-Cited by-同舟云学术

Hereditary spastic paraplegia and extensive leukoencephalopathy: a case report of a unique phenotype associated with a GJB1/Cx32 p.Pro174Ser variant

Published:2024-09-04 Issue:1 Volume:24 Page:
ISSN:1471-2377
Container-title:BMC Neurology
language:en
Short-container-title:BMC Neurol

Author:

Nakamura Haruko,Doi Hiroshi,Miyaji Yosuke,Wada Taishi,Takahashi Erisa,Tada Mikiko,Fukuda Hiromi,Fujita Atsushi,Higashiyama Yuichi,Nagao Yuri,Kimura Kazue,Hayashi Masaharu,Hoshino Kyoko,Matsumoto Naomichi,Tanaka Fumiaki

Publisher

Springer Science and Business Media LLC

Link

https://link.springer.com/content/pdf/10.1186/s12883-024-03823-9.pdf

Reference29 articles.

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