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

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

Book ID: 122623461
Publisher: Elsevier Science
Year: 2012
Tongue: English
Weight: 392 KB
Volume: 55
Category: Article
ISSN: 1769-7212
DOI: 10.1016/j.ejmg.2012.08.001

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