Article SCOPUS
Journal of Medical Case Reports  (2018)

Carnitine palmitoyltransferase type 2 deficiency: Novel mutation in a Native South American family with whole-body muscle magnetic resonance imaging findings: Two case reports

Avila-Smirnow, D.; Boutron A.; Beytía-Reyes M.D.L.Á.; Contreras-Olea O.; Caicedo-Feijoo A.; Gejman-Enríquez R.; Escobar-Henríquez R.; Förster-Mujica J.

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Título según SCOPUS: Carnitine palmitoyltransferase type 2 deficiency: Novel mutation in a Native South American family with whole-body muscle magnetic resonance imaging findings: Two case reports
Título de la Revista: Journal of Medical Case Reports
Volumen: 12
Número: 1
Editorial: BIOMED CENTRAL LTD
Fecha de publicación: 2018
Idioma: English
DOI:

10.1186/s13256-018-1702-3
Notas: SCOPUS