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Nashabat M, Al-Khenaizan S, Alfadhel M. Methionine adenosyltransferase I/III deficiency: beyond the central nervous system manifestations. Ther Clin Risk Manag. 2018;14:225-229doi: 10.2147/TCRM.S151732.
Nashabat, M., Al-Khenaizan, S., & Alfadhel, M. (2018). Methionine adenosyltransferase I/III deficiency: beyond the central nervous system manifestations. Therapeutics and clinical risk management, 14225-229. https://doi.org/10.2147/TCRM.S151732
Nashabat, Marwan, et al. "Methionine adenosyltransferase I/III deficiency: beyond the central nervous system manifestations." Therapeutics and clinical risk management vol. 14 (2018): 225-229. doi: https://doi.org/10.2147/TCRM.S151732
Nashabat M, Al-Khenaizan S, Alfadhel M. Methionine adenosyltransferase I/III deficiency: beyond the central nervous system manifestations. Ther Clin Risk Manag. 2018 Feb 02;14:225-229. doi: 10.2147/TCRM.S151732. eCollection 2018. PMID: 29440907; PMCID: PMC5798556.
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Ther Clin Risk Manag. 2018 Feb 02;14:225-229. doi: 10.2147/TCRM.S151732. eCollection 2018.

Methionine adenosyltransferase I/III deficiency: beyond the central nervous system manifestations.

Therapeutics and clinical risk management

Marwan Nashabat, Sultan Al-Khenaizan, Majid Alfadhel

Affiliations

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

PMID: 29440907 PMCID: PMC5798556 DOI: 10.2147/TCRM.S151732

Abstract

Methionine adenosyltransferase (MAT) I/III deficiency (OMIM # 250850) is caused by a mutation in

Keywords: MAT1A; S-adenosyl methionine; central nervous system; methionine adenosyltransferase

Conflict of interest statement

Disclosure The authors report no conflicts of interest in this work.

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