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Hipoplasia pontocerebelosa tipo I familiar con mutación en EXOSC3
Hipoplasia pontocerebelosa tipo I familiar con mutación en EXOSC3
2017
Anna Paola Di Giovambattista
Itxaropena Jácome Querejeta
Purificación Ventura Faci
Gerardo Rodríguez Martínez
Feliciano Jesús Ramos Fuentes
Keywords:
Medicine
Intensive care medicine
infant newborn
RNA-binding protein
Cerebellar diseases
Diabetes mellitus
fatal outcome
Bioinformatics
Exosome Multienzyme Ribonuclease Complex
Mutation
Correction
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