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Biallelic variants in the neuronal isoform of the DST gene as a cause of hereditary sensory neuropathy

; ; ; ; ;

In
Abstracts from the 57th European Society of Human Genetics (ESHG) Conference

In
European journal of human genetics 32(Supplement 2), Seiten/Artikel-Nr.:EP12.020

Konferenz/Event:57. Conference of the European-Society-of-Human-Genetics , Berlin , Germany , ESHG 2024 , 2024-06-01 - 2024-06-04

ImpressumBasingstoke : Stockton Press

Umfang1099-1099

ISSN1018-4813

e-Poster abstract. - In Artikel: Abstracts from the 57th European Society of Human Genetics (ESHG) Conference: e-Posters. - Seiten 904–1230

Online
URL: https://doi.org/10.1038/s41431-024-01733-5

Einrichtungen

  1. Institut und Lehrstuhl für Humangenetik und Genommedizin (924610)


Thematische Einordnung (Klassifikation)
DDC: 610

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Dokumenttyp
Abstract/Journal Article/Contribution to a conference proceedings

Format
online, print

Sprache
English

Anmerkung
No peer reviewed article

Externe Identnummern
WOS Core Collection: WOS:001421430500825

Interne Identnummern
RWTH-2025-10588
Datensatz-ID: 1023232

Beteiligte Länder
Czech Republic, Germany

Lizenzstatus der Zeitschrift

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The record appears in these collections:
Document types > Events > Contributions to a conference proceedings
Document types > Articles > Journal Articles
Document types > Presentations > Abstracts
Faculty of Medicine (Fac.10)
Public records
525000\-2
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 Record created 2025-12-10, last modified 2025-12-22


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