Dos nuevos casos de síndrome de Leigh por mutación m.13513G>A en el gen MTND5 / Two new cases of Leigh syndrome caused by mutation m.13513G> A in the MTND5 gene
Rev. neurol. (Ed. impr.)
; 68(7): 312-314, 1 abr., 2019.
Article
in Es
| IBECS
| ID: ibc-183316
Responsible library:
ES1.1
Localization: BNCS
RESUMEN
No disponible
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Collection:
06-national
/
ES
Database:
IBECS
Main subject:
Leigh Disease
/
Mutation
Limits:
Female
/
Humans
/
Infant
/
Male
/
Newborn
Language:
Es
Journal:
Rev. neurol. (Ed. impr.)
Year:
2019
Document type:
Article