The homozygous pathogenic variant of the POMGNT1 gene identified using whole-exome sequencing in Iranian family with congenital hydrocephalus
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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1 Online-Ressource.
- Sprache
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Englisch
- Erschienen in
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The homozygous pathogenic variant of the POMGNT1 gene identified using whole-exome sequencing in Iranian family with congenital hydrocephalus ; volume:25 ; number:1 ; day:26 ; month:3 ; year:2024 ; pages:1-13 ; date:12.2024
The Egyptian journal of medical human genetics ; 25, Heft 1 (26.3.2024), 1-13, 12.2024
- Urheber
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Sabzeghabaiean, Masoud
Maleknia, Mohsen
Mohammadi-Asl, Javad
Kazemi, Hashem
Golab, Fereshteh
Zargar, Zohreh
Naseroleslami, Maryam
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1186/s43042-024-00513-6
- URN
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urn:nbn:de:101:1-2406121202127.968114813539
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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14.08.2025, 10:52 MESZ
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Beteiligte
- Sabzeghabaiean, Masoud
- Maleknia, Mohsen
- Mohammadi-Asl, Javad
- Kazemi, Hashem
- Golab, Fereshteh
- Zargar, Zohreh
- Naseroleslami, Maryam
- SpringerLink (Online service)
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