スポンサーリンク
Human Genome Center, School of Medical Sciences, Universiti Sains Malaysia | 論文
- Screening of the LIX1 gene in Japanese and Malaysian patients with SMA and/or SMA-like disorder
- Combination of SMN2 copy number and NAIP deletion predicts disease severity in spinal muscular atrophy
- Contribution of MSX1 variants to the risk of non-syndromic cleft lip and palate in a Malay population