An incidental finding in newborn screening leading to the diagnosis of a patient with ECHS1 mutations
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J. A. Arranz | F. Tort | A. Ribes | L. Gort | O. Ugarteburu | M. del Toro | J. Marín | R. M. López | J. García-Villoria | A. Argudo-Ramírez | S. Pajares | R. Fernández | J. M. González de Aledo-Castillo | M.D. Casellas