Morino, H., Miyamoto, R., Ohnishi, S., Maruyama, H., & Kawakami, H. (2014). Exome sequencing reveals a novel TTC19 mutation in an autosomal recessive spinocerebellar ataxia patient. BioMed Central.
Citação norma ChicagoMorino, Hiroyuki, Ryosuke Miyamoto, Shizuo Ohnishi, Hirofumi Maruyama, and Hideshi Kawakami. Exome Sequencing Reveals a Novel TTC19 Mutation in an Autosomal Recessive Spinocerebellar Ataxia Patient. BioMed Central, 2014.
ציטוט MLAMorino, Hiroyuki, et al. Exome Sequencing Reveals a Novel TTC19 Mutation in an Autosomal Recessive Spinocerebellar Ataxia Patient. BioMed Central, 2014.
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