Phenotypic variability in a Tunisian family with X-linked adrenoleukodystrophy caused by the p.Gln316Pro novel mutation

• 期刊名称Clinica Chimica Acta
• 作者Kallabi, Fakhri; Ellouz, Emna; Tabebi, Mouna; Ben Salah, Ghada; Kaabechi, Naziha; Keskes, Leila; Triki, Chahnez; Kamoun, Hassen
• 卷第453卷
• 印刷ISSN0009-8981
• 文件大小1338.28KB
• 发表时间2016-01
• DOI10.1016/j.cca.2015.12.014
• 页码141-146