Gene identification in the congenital disorders of glycosylation type I by whole-exome sequencing
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A. Hoischen | J. Veltman | R. Rodenburg | C. Gilissen | E. Jamroz | R. Wevers | C. Thiel | E. Morava | D. Lefeber | Ilse Eidhof | L. Heuvel | J. Paprocka | M. Adamowicz | C. Körner | L. Lehle | S. Timal | K. Huijben | J. Sykut-Cegielska | F. V. Spronsen | Karin Huijben