论文信息 - The E37X is a common HMGCL mutation in Portuguese patients with 3-hydroxy-3-methylglutaric CoA lyase deficiency. - 字舞流文

The E37X is a common HMGCL mutation in Portuguese patients with 3-hydroxy-3-methylglutaric CoA lyase deficiency.

M. Rolland | M. L. Cardoso | M. R. Rodrigues | E. Leão | E. Martins | L. Diogo | E. Rodrigues | P. Garcia | L. Vilarinho