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Browsing by Author Amiel, J.
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2010
IDH2 mutations in patients with D-2-hydroxyglutaric aciduria.
Kranendijk, M.
;
Struys, E.A.
;
Schaftingen, E. van
, et al
2006
Loss-of-function mutations in euchromatin histone methyl transferase 1 (EHMT1) cause the 9q34 subtelomeric deletion syndrome.
Kleefstra, T.
;
Brunner, H.G.
;
Amiel, J.
, et al
Showing results 1 to 2 of 2
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