A novel missense mutation of FOXC1 in an Axenfeld–Rieger syndrome patient with a congenital atrial septal defect and sublingual cyst: a case report and literature review

Location
Deutsche Nationalbibliothek Frankfurt am Main
ISSN
1755-8794
Extent
Online-Ressource
Language
Englisch
Notes
online resource.

Bibliographic citation
A novel missense mutation of FOXC1 in an Axenfeld–Rieger syndrome patient with a congenital atrial septal defect and sublingual cyst: a case report and literature review ; volume:14 ; number:1 ; day:29 ; month:10 ; year:2021 ; pages:1-10 ; date:12.2021
BMC medical genomics ; 14, Heft 1 (29.10.2021), 1-10, 12.2021

Creator
Li, Kaiming
Tang, Min
Xu, Manhua
Yu, Yinggui
Contributor
SpringerLink (Online service)

DOI
10.1186/s12920-021-01103-w
URN
urn:nbn:de:101:1-2022010821004770738287
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
15.08.2025, 7:23 AM CEST

Data provider

This object is provided by:
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Associated

  • Li, Kaiming
  • Tang, Min
  • Xu, Manhua
  • Yu, Yinggui
  • SpringerLink (Online service)

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