JESÚS
GARDEAZABAL GARCÍA
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Necker-Enfants Malades Hospital
París, FranciaPublicaciones en colaboración con investigadores/as de Necker-Enfants Malades Hospital (1)
2016
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Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencing
Orphanet Journal of Rare Diseases, Vol. 11, Núm. 1