المؤلفون: Houten, S.M. (Sander M.), Te Brinke, H. (Heleen), Denis, S. (Simone), Ruiter, J.P.N. (Jos), Knegt, A.C. (Alida), Klerk, J.B.C. (Johannes) de, Augoustides-Savvopoulou, P. (Persa), Häberle, J. (Johannes), Baumgartner, M.R. (Matthias), Coşkun, T. (Turgay), Zschocke, J. (Johannes), Sass, J.O. (Jörn Oliver), Poll-The, B.T., Wanders, R.J.A. (Ronald), Duran, M. (Marinus)

المصدر: Orphanet Journal of Rare Diseases vol. 8 no. 1

مصطلحات موضوعية: Contiguous gene deletion syndrome, Hyperlysinemia, Inborn errors of metabolism, Lysine

وصف الملف: application/pdf

Relation: http://repub.eur.nl/pub/61443; urn:hdl:1765/61443

الاتاحة: http://repub.eur.nl/pub/61443
https://doi.org/10.1186/1750-1172-8-57