Mutations in ATP1A3 cause alternating hemiplegia of childhood

10.1111/cge.12031

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Bibliographic Details
Main Author:	Aminkeng, F
Other Authors:	MEDICINE
Format:	Editorial
Language:	English
Published:	WILEY 2022
Subjects:	Science & Technology Life Sciences & Biomedicine Genetics & Heredity ONSET
Online Access:	https://scholarbank.nus.edu.sg/handle/10635/235311
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Institution:	National University of Singapore
Language:	English

id	sg-nus-scholar.10635-235311
record_format	dspace
spelling	sg-nus-scholar.10635-2353112024-04-17T08:36:33Z Mutations in ATP1A3 cause alternating hemiplegia of childhood Aminkeng, F MEDICINE Science & Technology Life Sciences & Biomedicine Genetics & Heredity ONSET 10.1111/cge.12031 CLINICAL GENETICS 83 1 32-33 2022-12-05T03:28:28Z 2022-12-05T03:28:28Z 2013-01-01 2022-11-30T19:43:59Z Editorial Aminkeng, F (2013-01-01). Mutations in ATP1A3 cause alternating hemiplegia of childhood. CLINICAL GENETICS 83 (1) : 32-33. ScholarBank@NUS Repository. https://doi.org/10.1111/cge.12031 0009-9163 1399-0004 https://scholarbank.nus.edu.sg/handle/10635/235311 en WILEY Elements
institution	National University of Singapore
building	NUS Library
continent	Asia
country	Singapore Singapore
content_provider	NUS Library
collection	ScholarBank@NUS
language	English
topic	Science & Technology Life Sciences & Biomedicine Genetics & Heredity ONSET
spellingShingle	Science & Technology Life Sciences & Biomedicine Genetics & Heredity ONSET Aminkeng, F Mutations in ATP1A3 cause alternating hemiplegia of childhood
description	10.1111/cge.12031
author2	MEDICINE
author_facet	MEDICINE Aminkeng, F
format	Editorial
author	Aminkeng, F
author_sort	Aminkeng, F
title	Mutations in ATP1A3 cause alternating hemiplegia of childhood
title_short	Mutations in ATP1A3 cause alternating hemiplegia of childhood
title_full	Mutations in ATP1A3 cause alternating hemiplegia of childhood
title_fullStr	Mutations in ATP1A3 cause alternating hemiplegia of childhood
title_full_unstemmed	Mutations in ATP1A3 cause alternating hemiplegia of childhood
title_sort	mutations in atp1a3 cause alternating hemiplegia of childhood
publisher	WILEY
publishDate	2022
url	https://scholarbank.nus.edu.sg/handle/10635/235311
_version_	1800915748684562432

Mutations in ATP1A3 cause alternating hemiplegia of childhood

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