Clinical and molecular analysis of isovaleric acidemia patients in the United Arab Emirates reveals remarkable phenotypes and four novel mutations in the IVD gene

Jozef L. Hertecant, Imen Ben-Rebeh, Muhaned A. Marah, Thikra Abbas, Leila Ayadi, Salma Ben Salem, Fatma A. Al-Jasmi, Lihadh Al-Gazali, Said A. Al-Yahyaee, Bassam R. Ali^*

^*المؤلف المقابل لهذا العمل