A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disability
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1755-8794
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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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
- Creator
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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
- Contributor
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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
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:24 AM CEST
Data provider
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Associated
- 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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