Thyroid involvement in Chanarin-Dorfman syndrome in adults in the largest series of patients carrying the same founder mutation in ABHD5 gene

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Standort
Deutsche Nationalbibliothek Frankfurt am Main
ISSN
1750-1172
Umfang
Online-Ressource
Sprache
Englisch
Anmerkungen
online resource.

Erschienen in
Thyroid involvement in Chanarin-Dorfman syndrome in adults in the largest series of patients carrying the same founder mutation in ABHD5 gene ; volume:14 ; number:1 ; day:22 ; month:5 ; year:2019 ; pages:1-8 ; date:12.2019
Orphanet journal of rare diseases ; 14, Heft 1 (22.5.2019), 1-8, 12.2019

Urheber
Louhichi, Nacim
Bahloul, Emna
Marrakchi, Slaheddine
Othman, Houda Ben
Triki, Chahnez
Aloulou, Kawthar
Trabelsi, Lobna
Mahfouth, Nadia
Ayadi-Mnif, Zeineb
Keskes, Leila
Fakhfakh, Faiza
Turki, Hamida
Beteiligte Personen und Organisationen
SpringerLink (Online service)

DOI
10.1186/s13023-019-1095-4
URN
urn:nbn:de:101:1-2019110713490477764562
Rechteinformation
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Letzte Aktualisierung
15.08.2025, 07:35 MESZ

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Beteiligte

  • Louhichi, Nacim
  • Bahloul, Emna
  • Marrakchi, Slaheddine
  • Othman, Houda Ben
  • Triki, Chahnez
  • Aloulou, Kawthar
  • Trabelsi, Lobna
  • Mahfouth, Nadia
  • Ayadi-Mnif, Zeineb
  • Keskes, Leila
  • Fakhfakh, Faiza
  • Turki, Hamida
  • SpringerLink (Online service)

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