Clinical and genetic analysis of two wolfram syndrome families with high occurrence of wolfram syndrome and diabetes type II: a case report
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1471-2350
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Clinical and genetic analysis of two wolfram syndrome families with high occurrence of wolfram syndrome and diabetes type II: a case report ; volume:21 ; number:1 ; day:14 ; month:1 ; year:2020 ; pages:1-8 ; date:12.2020
BMC medical genetics ; 21, Heft 1 (14.1.2020), 1-8, 12.2020
- Urheber
-
Sobhani, Maryam
Tabatabaiefar, Mohammad Amin
Ghafouri-Fard, Soudeh
Rajab, Asadollah
Hojjat, Asal
Kajbafzadeh, Abdol-Mohammad
Noori-Daloii, Mohammad Reza
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1186/s12881-020-0950-4
- URN
-
urn:nbn:de:101:1-2020061700283512746473
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:49 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Sobhani, Maryam
- Tabatabaiefar, Mohammad Amin
- Ghafouri-Fard, Soudeh
- Rajab, Asadollah
- Hojjat, Asal
- Kajbafzadeh, Abdol-Mohammad
- Noori-Daloii, Mohammad Reza
- SpringerLink (Online service)
Ähnliche Objekte (12)
Correction to: Clinical and genetic analysis of two wolfram syndrome families with high occurrence of wolfram syndrome and diabetes type II: a case report
Wolfram syndrome: MAMs’ connection?
Phenotypic characteristics of early Wolfram syndrome
Taste and smell function in Wolfram syndrome
Sleep disturbances in Wolfram syndrome
Selective cognitive and psychiatric manifestations in Wolfram Syndrome
Early presentation of gait impairment in Wolfram Syndrome
Longitudinal hearing loss in Wolfram syndrome
EURO-WABB: an EU rare diseases registry for Wolfram syndrome, Alström syndrome and Bardet-Biedl syndrome
Wolfram syndrome type 1: a case series
Neuronal calcium sensor 1-dependent signaling in Wolfram syndrome and cognitive impairment
Evidence for altered neurodevelopment and neurodegeneration in Wolfram syndrome using longitudinal morphometry
Correction to: Clinical and genetic analysis of two wolfram syndrome families with high occurrence of wolfram syndrome and diabetes type II: a case report
Wolfram syndrome: MAMs’ connection?
Phenotypic characteristics of early Wolfram syndrome
Taste and smell function in Wolfram syndrome
Sleep disturbances in Wolfram syndrome
Selective cognitive and psychiatric manifestations in Wolfram Syndrome
Early presentation of gait impairment in Wolfram Syndrome
Longitudinal hearing loss in Wolfram syndrome
EURO-WABB: an EU rare diseases registry for Wolfram syndrome, Alström syndrome and Bardet-Biedl syndrome
Wolfram syndrome type 1: a case series
Neuronal calcium sensor 1-dependent signaling in Wolfram syndrome and cognitive impairment
Evidence for altered neurodevelopment and neurodegeneration in Wolfram syndrome using longitudinal morphometry
Correction to: Clinical and genetic analysis of two wolfram syndrome families with high occurrence of wolfram syndrome and diabetes type II: a case report
Wolfram syndrome: MAMs’ connection?
Phenotypic characteristics of early Wolfram syndrome
Taste and smell function in Wolfram syndrome
Sleep disturbances in Wolfram syndrome
Selective cognitive and psychiatric manifestations in Wolfram Syndrome
Early presentation of gait impairment in Wolfram Syndrome
Longitudinal hearing loss in Wolfram syndrome
EURO-WABB: an EU rare diseases registry for Wolfram syndrome, Alström syndrome and Bardet-Biedl syndrome
Wolfram syndrome type 1: a case series
Neuronal calcium sensor 1-dependent signaling in Wolfram syndrome and cognitive impairment