Two novel variants in DYRK1B causative of AOMS3: expanding the clinical spectrum
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1750-1172
- 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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Two novel variants in DYRK1B causative of AOMS3: expanding the clinical spectrum ; volume:16 ; number:1 ; day:30 ; month:6 ; year:2021 ; pages:1-10 ; date:12.2021
Orphanet journal of rare diseases ; 16, Heft 1 (30.6.2021), 1-10, 12.2021
- Urheber
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Mendoza-Caamal, Elvia C.
Barajas-Olmos, Francisco
Mirzaeicheshmeh, Elaheh
Ilizaliturri-Flores, Ian
Aguilar-Salinas, Carlos A.
Gómez-Velasco, Donaji V.
Cicerón-Arellano, Isabel
Reséndiz-Rodríguez, Adriana
Martínez-Hernández, Angélica
Contreras-Cubas, Cecilia
Islas-Andrade, Sergio
Zerrweck, Carlos
García-Ortiz, Humberto
Orozco, Lorena
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1186/s13023-021-01924-z
- URN
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urn:nbn:de:101:1-2021101221243738718260
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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15.08.2025, 08:24 MESZ
Datenpartner
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Beteiligte
- Mendoza-Caamal, Elvia C.
- Barajas-Olmos, Francisco
- Mirzaeicheshmeh, Elaheh
- Ilizaliturri-Flores, Ian
- Aguilar-Salinas, Carlos A.
- Gómez-Velasco, Donaji V.
- Cicerón-Arellano, Isabel
- Reséndiz-Rodríguez, Adriana
- Martínez-Hernández, Angélica
- Contreras-Cubas, Cecilia
- Islas-Andrade, Sergio
- Zerrweck, Carlos
- García-Ortiz, Humberto
- Orozco, Lorena
- SpringerLink (Online service)
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