A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disability
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1755-8794
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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online resource.
- Erschienen in
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A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disability ; volume:15 ; number:1 ; day:8 ; month:11 ; year:2022 ; pages:1-5 ; date:12.2022
BMC medical genomics ; 15, Heft 1 (8.11.2022), 1-5, 12.2022
- Urheber
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Amin, Mutaz
Vignal, Cedric
Eltaraifee, Esraa
Mohammed, Inaam N.
Hamed, Ahlam A. A.
Elseed, Maha A.
Babai, Arwa
Elbadi, Iman
Mustafa, Doua
Abubaker, Rayan
Mustafa, Mohamed
Drunat, Severine
Elsayed, Liena E. O.
Ahmed, Ammar E.
Boespflug-Tanguy, Odile
Dorboz, Imen
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1186/s12920-022-01354-1
- URN
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urn:nbn:de:101:1-2023012210202674472175
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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15.08.2025, 07:24 MESZ
Datenpartner
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Beteiligte
- Amin, Mutaz
- Vignal, Cedric
- Eltaraifee, Esraa
- Mohammed, Inaam N.
- Hamed, Ahlam A. A.
- Elseed, Maha A.
- Babai, Arwa
- Elbadi, Iman
- Mustafa, Doua
- Abubaker, Rayan
- Mustafa, Mohamed
- Drunat, Severine
- Elsayed, Liena E. O.
- Ahmed, Ammar E.
- Boespflug-Tanguy, Odile
- Dorboz, Imen
- SpringerLink (Online service)
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