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J Cent Nerv Syst Dis. 2017 Oct 27;9:1179573517737521. doi: 10.1177/1179573517737521. eCollection 2017.

Early Infantile Leigh-like .

Journal of central nervous system disease

Majid Alfadhel

Affiliations

  1. King Abdullah International Medical Research Centre, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
  2. Division of Genetics, Department of Pediatrics, King Abdulaziz Medical City, Ministry of National Guard-Health Affairs (NGHA), Riyadh, Saudi Arabia.

PMID: 29123435 PMCID: PMC5661663 DOI: 10.1177/1179573517737521

Abstract

Solute carrier family 19 (thiamine transporter), member 3 (

Keywords: Leigh syndrome; Leigh-like; SCL19A3 gene defect; SLC19A3 gene; biotin; thiamine

Conflict of interest statement

Declaration of conflicting interests:The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

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