OpenCitations

Genetic screening of ATP7B gene in Iranian Wilson disease patients: a diverse landscape of pathogenic variants

Egyptian Journal of Medical Human Genetics 26(1) (2025)

Seyyed-Saleh Hashemi; Seyed Ali Jafari; Aida Gholoobi; Tayebeh Hamzehloei

Gene mutations in Wilson disease in Egyptian children: Report on two novel mutations

Arab Journal of Gastroenterology 15(3-4) (2014)

Fatma A. El-Mougy; Sahar A.A. Sharaf; Marwa M. Elsharkawy; Iman A. Mandour; Riham A. El-Essawy; Abeer M. Eldin; Heba M. Helmy; Dina H. Soliman; Lamia H. Selim; Heba M. Sharafeldin; Engy A. Mogahed; Hanaa M. El-Karaksy

Novel compound heterozygote mutations in the ATP7B gene in an Iranian family with Wilson disease: a case report

Journal of Medical Case Reports 12(1) (2018)

Omid Daneshjoo; Masoud Garshasbi

Wilson’s disease in Lebanon and regional countries: Homozygosity and hepatic phenotype predominance

World Journal of Gastroenterology 23(36) (2017)

Kassem Barada; Aline El Haddad; Meghri Katerji; Mustapha Jomaa; Julnar Usta

Geographic distribution of ATP7B mutations in Wilson disease

Annals of Human Biology 43(1) (2015)

Amanda Gomes; George V. Dedoussis

Multiplex ARMS PCR to Detect 8 Common Mutations of ATP7B Gene in Patients With Wilson Disease

Hepatitis Monthly 13(5) (2013)

Hassan Dastsooz; Mohammad Hadi; Seyed Mohsen; Mahmood Haghighat; Maryam Moini; Majid Fardaei

The genetics of Wilson disease

Handbook of Clinical Neurology (2017)