A novel SCN9A gene variant identified in a Chinese girl with paroxysmal extreme pain disorder (PEPD): a rare case report
- 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 SCN9A gene variant identified in a Chinese girl with paroxysmal extreme pain disorder (PEPD): a rare case report ; volume:15 ; number:1 ; day:15 ; month:7 ; year:2022 ; pages:1-6 ; date:12.2022
BMC medical genomics ; 15, Heft 1 (15.7.2022), 1-6, 12.2022
- Urheber
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Hua, Yi
Cui, Di
Han, Lin
Xu, Lu
Mao, Shanshan
Yang, Cuiwei
Gao, Feng
Yuan, Zhefeng
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1186/s12920-022-01302-z
- URN
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urn:nbn:de:101:1-2022092106212018726176
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
- 15.08.2025, 07:20 MESZ
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Beteiligte
- Hua, Yi
- Cui, Di
- Han, Lin
- Xu, Lu
- Mao, Shanshan
- Yang, Cuiwei
- Gao, Feng
- Yuan, Zhefeng
- SpringerLink (Online service)
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