Phenotype-Genotype Correlation in Wilson Disease in a Large Lebanese Family: Association of c.2299insC with Hepatic and of p. Ala1003Thr with Neurologic Phenotype

por Usta, Julnar, Wehbeh, Antonios, Rida, Khaled, El-Rifai, Omar, Estiphan, Theresa Alicia, Majarian, Tamar, Barada, Kassem
Publicado 2014