Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Najwa Imad"'
Autor:
Karima Lafhal, Es-said Sabir, Abdelmalek Hakmaoui, Miloud Hammoud, Abdelmohcine Aimrane, Samira Najeh, Imane Assiri, Abdelaati Berrachid, Najwa Imad, Chaima Ait Boujemaa, Faissal Aziz, Fatima Zahra El Hanafi, Abdessamad Lalaoui, Hasna Aamri, Iryna Boyko, Ana Sánchez-Monteagudo, Carmen Espinós, Imane Ait Sab, Nisrine Aboussair, Aicha Bourrahouat, Naima Fdil
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 36, Iss , Pp 100984- (2023)
Background: Wilson Disease (WD) is an autosomal recessive inherited metabolic disease caused by mutations in the ATP7B gene. WD is characterized by heterogeneous clinical presentations expressed by hepatic and neuropsychiatric phenotypes. The disease
Externí odkaz:
https://doaj.org/article/2b5a71fe814d4cfc853165f69d5a9f6a
Publikováno v:
HIV Nursing; 2023, Vol. 23 Issue 1, p402-406, 5p