Ciliary and centrosomal defects associated with mutation and depletion of the Meckel syndrome genes MKS1 and MKS3.
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V. Torres | P. Harris | V. Gattone | C. Ward | Rachel M. Sinders | P. Czarnecki | Cynthia J. Hommerding | A. Leightner | Caroline A. Miller | J. Salisbury | R. Tammachote | Rachel M Sinders