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Mutational spectrum of COH1 and clinical heterogeneity in Cohen syndrome.
W. Seifert, M. Holder-Espinasse, S. Spranger, M. Hoeltzenbein, E. Rossier, H. Dollfus, D. Lacombe, A. Verloes, K. H. Chrzanowska, G. H. Maegawa, D. Chitayat, D. Kotzot, D. Huhle, P. Meinecke, B. Albrecht, I. Mathijssen, B. Leheup, K. Raile, H. C. Hennies, D. Horn
Research output: Contribution to journal › Letter › peer-review
44
Scopus
citations