Whole Exome Sequencing Is the Preferred Strategy to Identify the Genetic Defect in Patients With a Probable or Possible Mitochondrial Cause
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H. Smeets | R. Kamps | B. de Koning | Y. Hilhorst‐Hofstee | R. Szklarczyk | M. de Visser | S. Sallevelt | Ralph W. H. Gottschalk | D. Hellebrekers | J. Vanoevelen | I. D. de Coo | M. Gerards | S. Fuchs | Tom E. J. Theunissen | K. Schoonderwoerd | A. Stassen | A. Hendrickx | M. Nguyen | C. Calis | Elvira N. M. Mulder-Den Hartog | Chantal Calis | Mike Gerards | Irenaeus F. M. de Coo | Y. Hilhorst-Hofstee