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

Nashabat, Marwan; Al-Khenaizan, Sultan; Alfadhel, Majid

Nashabat, Marwan; Al-Khenaizan, Sultan; Alfadhel, Majid.

Afiliación

Nashabat M; 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.
Al-Khenaizan S; 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.
Alfadhel M; 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.

Ther Clin Risk Manag ; 14: 225-229, 2018.

Article en En | MEDLINE | ID: mdl-29440907

Palabras clave

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

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Ther Clin Risk Manag Año: 2018 Tipo del documento: Article País de afiliación: Arabia Saudita

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