论文信息 - Mutational analysis of COQ2 in patients with MSA in Italy - 字舞流文

Mutational analysis of COQ2 in patients with MSA in Italy

N. Bresolin | G. Comi | S. Corti | A. Priori | G. Mora | F. Cogiamanian | G. Ardolino | B. Garavaglia | A. Elia | A. Fonzo | E. Monfrini | C. Bergamini | R. Fato | F. Fortunato | G. Franco | V. Melzi | G. Compagnoni | S. Bonato | C. Barzaghi | D. Ronchi | R. Bo | L. Borellini | Emanuele Frattini | F. Sorbo | E. D. Biase | I. Trezzi

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[4] P Sandroni,et al. Second consensus statement on the diagnosis of multiple system atrophy , 2008, Neurology.

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[6] S. Dimauro,et al. A mutation in para-hydroxybenzoate-polyprenyl transferase (COQ2) causes primary coenzyme Q10 deficiency. , 2006, American journal of human genetics.