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Biallelic loss-of-function variants of ZFTRAF1 cause neurodevelopmental disorder with microcephaly and hypotonia

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In
Neurology

In
Genetics in medicine 26(7), Seiten/Artikel-Nr.:101143

ImpressumAmsterdam : Elsevier

Umfang[1]-16

ISSN1530-0366

Online
DOI: 10.1016/j.gim.2024.101143

DOI: 10.18154/RWTH-CONV-253568
URL: https://publications.rwth-aachen.de/record/1007214/files/1007214.pdf

Einrichtungen

  1. Institut und Lehrstuhl für Humangenetik und Genommedizin (525000-2)


OpenAccess:
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Dokumenttyp
Journal Article/Contribution to a book

Format
online, print

Sprache
English

Anmerkung
Peer reviewed article

Externe Identnummern
SCOPUS: SCOPUS:2-s2.0-85193293159
WOS Core Collection: WOS:001245869800001
PubMed: pmid:38641995

Interne Identnummern
RWTH-CONV-253568
Datensatz-ID: 1007214

Beteiligte Länder
Germany, Pakistan, Saudi Arabia, Spain

Lizenzstatus der Zeitschrift

 GO


Medline ; Creative Commons Attribution-NonCommercial-NoDerivs CC BY-NC-ND 4.0 ; OpenAccess ; BIOSIS Previews ; Biological Abstracts ; Clarivate Analytics Master Journal List ; Current Contents - Clinical Medicine ; DEAL Springer ; Essential Science Indicators ; IF >= 5 ; JCR ; NationallizenzNationallizenz ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection

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Document types > Articles > Journal Articles
Publication server / Open Access
Faculty of Medicine (Fac.10)
Public records
525000\-2
Publications database

 Record created 2025-03-18, last modified 2025-09-29


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