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Dive into the research topics of 'Novel exon 1 mutations in MECP2 implicate isoform MeCP2-e1 in classical rett syndrome'. Together they form a unique fingerprint.- Sort by
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Carol J. Saunders, Berge E. Minassian, Eva W.C. Chow, Weiwei Zhao, John B. Vincent
Research output: Contribution to journal › Article › peer-review