Novel homozygous variant in the TPO gene associated with congenital hypothyroidism and mild-intellectual disability
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2054-345X
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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online resource.
- Erschienen in
-
Novel homozygous variant in the TPO gene associated with congenital hypothyroidism and mild-intellectual disability ; volume:7 ; number:1 ; day:27 ; month:11 ; year:2020 ; pages:1-4 ; date:12.2020
Human genome variation ; 7, Heft 1 (27.11.2020), 1-4, 12.2020
- Urheber
-
Khan, Amjad
Umair, Muhammad
Sharaf, Rania Abdulfattah
Khan, Muhammad Ismail
Ullah, Amir
Abbas, Safdar
Shaheen, Nargis
Bilal, Muhammad
Ahamd, Farooq
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
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10.1038/s41439-020-00129-3
- URN
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urn:nbn:de:101:1-2021010718335991417114
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:27 MESZ
Datenpartner
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Beteiligte
- Khan, Amjad
- Umair, Muhammad
- Sharaf, Rania Abdulfattah
- Khan, Muhammad Ismail
- Ullah, Amir
- Abbas, Safdar
- Shaheen, Nargis
- Bilal, Muhammad
- Ahamd, Farooq
- SpringerLink (Online service)
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