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

id	sg-nus-scholar.10635-243222
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spelling	sg-nus-scholar.10635-2432222024-04-02T23:51:20Z Autonomic dysfunction-dominant phenotype in a Chinese family with biallelic GGC repeat expansions in NOTCH2NLC Chen, B Jing, J Dong, G Shi, Y Zhang, C Zhang, Y Wang, A Tai, H Niu, S Wang, X Pan, H Zhang, Z CHINESE STUDIES 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 10.1007/s10072-023-06688-x Neurological Sciences 44 5 1769-1772 2023-07-19T09:11:37Z 2023-07-19T09:11:37Z 2023-05-01 2023-07-19T07:50:50Z Article Chen, B, Jing, J, Dong, G, Shi, Y, Zhang, C, Zhang, Y, Wang, A, Tai, H, Niu, S, Wang, X, Pan, H, Zhang, Z (2023-05-01). Autonomic dysfunction-dominant phenotype in a Chinese family with biallelic GGC repeat expansions in NOTCH2NLC. Neurological Sciences 44 (5) : 1769-1772. ScholarBank@NUS Repository. https://doi.org/10.1007/s10072-023-06688-x 1590-1874 1590-3478 https://scholarbank.nus.edu.sg/handle/10635/243222 Springer Science and Business Media LLC Elements
institution	National University of Singapore
building	NUS Library
continent	Asia
country	Singapore Singapore
content_provider	NUS Library
collection	ScholarBank@NUS
topic	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
spellingShingle	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 Chen, B Jing, J Dong, G Shi, Y Zhang, C Zhang, Y Wang, A Tai, H Niu, S Wang, X Pan, H Zhang, Z Autonomic dysfunction-dominant phenotype in a Chinese family with biallelic GGC repeat expansions in NOTCH2NLC
description	10.1007/s10072-023-06688-x
author2	CHINESE STUDIES
author_facet	CHINESE STUDIES Chen, B Jing, J Dong, G Shi, Y Zhang, C Zhang, Y Wang, A Tai, H Niu, S Wang, X Pan, H Zhang, Z
format	Article
author	Chen, B Jing, J Dong, G Shi, Y Zhang, C Zhang, Y Wang, A Tai, H Niu, S Wang, X Pan, H Zhang, Z
author_sort	Chen, B
title	Autonomic dysfunction-dominant phenotype in a Chinese family with biallelic GGC repeat expansions in NOTCH2NLC
title_short	Autonomic dysfunction-dominant phenotype in a Chinese family with biallelic GGC repeat expansions in NOTCH2NLC
title_full	Autonomic dysfunction-dominant phenotype in a Chinese family with biallelic GGC repeat expansions in NOTCH2NLC
title_fullStr	Autonomic dysfunction-dominant phenotype in a Chinese family with biallelic GGC repeat expansions in NOTCH2NLC
title_full_unstemmed	Autonomic dysfunction-dominant phenotype in a Chinese family with biallelic GGC repeat expansions in NOTCH2NLC
title_sort	autonomic dysfunction-dominant phenotype in a chinese family with biallelic ggc repeat expansions in notch2nlc
publisher	Springer Science and Business Media LLC
publishDate	2023
url	https://scholarbank.nus.edu.sg/handle/10635/243222
_version_	1795302013073883136

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

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