Associated Papers
Clinical and molecular analysis of isovaleric acidemia patients in the United Arab Emirates reveals remarkable phenotypes and four novel mutations in the IVD gene.
Hertecant JL et al.
European Journal of Medical Genetics, 2012
Phenotypic and mutation spectrums of Thai patients with isovaleric acidemia.
Vatanavicharn N et al.
Pediatrics International : Official Journal of the Japan Pediatric Society, 2011
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