Pennings, M., Schouten, M. I., van Gaalen, J., Meijer, R. P. P., de Bot, S. T., Kriek, M., . . . Kamsteeg, E. (2019). KIF1A variants are a frequent cause of autosomal dominant hereditary spastic paraplegia. Eur J Hum Genet.
シカゴスタイル引用形Pennings, Maartje, et al. "KIF1A Variants Are a Frequent Cause of Autosomal Dominant Hereditary Spastic Paraplegia." Eur J Hum Genet 2019.
MLA引用形式Pennings, Maartje, et al. "KIF1A Variants Are a Frequent Cause of Autosomal Dominant Hereditary Spastic Paraplegia." Eur J Hum Genet 2019.
警告: この引用は必ずしも正確ではありません.