Autonomic dysfunction-dominant phenotype in a Chinese family with biallelic GGC repeat expansions in NOTCH2NLC

Autonomic dysfunction-dominant phenotype in a Chinese family with biallelic GGC repeat expansions in NOTCH2NLC

10.1007/s10072-023-06688-x

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Bibliographic Details
Main Authors:	Chen, B, Jing, J, Dong, G, Shi, Y, Zhang, C, Zhang, Y, Wang, A, Tai, H, Niu, S, Wang, X, Pan, H, Zhang, Z
Other Authors:	CHINESE STUDIES
Format:	Article
Published:	Springer Science and Business Media LLC 2023
Subjects:	Autonomic dysfunction Biallelic GGC repeat expansions Deep medullary veins NOTCH2NLC Neuronal intranuclear inclusion disease Humans Autonomic Nervous System Diseases Brain East Asian People Intranuclear Inclusion Bodies Neurodegenerative Diseases Phenotype Trinucleotide Repeat Expansion Nerve Tissue Proteins Intercellular Signaling Peptides and Proteins
Online Access:	https://scholarbank.nus.edu.sg/handle/10635/243222
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Institution:	National University of Singapore

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