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*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

16 Citations (Scopus)

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