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Updated: Feb 19, 2026

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
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Early Infantile Leigh-like SLC19A3 Gene Defects Have a Poor Prognosis: Report and Review

Majid Alfadhel1,2

  • 1King Abdullah International Medical Research Centre, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.

Journal of Central Nervous System Disease
|November 11, 2017
PubMed

Keywords:
Leigh syndromeLeigh-likeSCL19A3 gene defectSLC19A3 genebiotinthiamine

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