Nueva mutación en el gen KMT2B como causa de distonía generalizada de inicio temprano: reporte de caso

Rangel, Yully Andrea; Espinosa, Eugenia.
Biomédica (Bogotá) ; 42(3): 429-434, jul.-set. 2022. tab
Artigo em Espanhol | LILACS | ID: biblio-1403593

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