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	1.	Pmp22 mutant allele-specific siRNA alleviates demyelinating neuropathic phenotype in vivo. [electronic resource] by Lee, Ji-Su Chang, Eun Hyuk Koo, Ok Jae Jwa, Dong Hwan Mo, Won Min Kwak, Geon Moon, Hyo Won Park, Hwan Tae Hong, Young Bin Choi, Byung-Ok Producer: 20180222 In: Neurobiology of disease vol. 100 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	A novel homozygous MPV17 mutation in two families with axonal sensorimotor polyneuropathy. [electronic resource] by Choi, Yu-Ri Hong, Young Bin Jung, Sung-Chul Lee, Ja Hyun Kim, Ye Jin Park, Hyung Jun Lee, Jinho Koo, Heasoo Lee, Ji-Su Jwa, Dong Hwan Jung, Namhee Woo, So-Youn Kim, Sang-Beom Chung, Ki Wha Choi, Byung-Ok Producer: 20160525 In: BMC neurology vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A Mutation in PMP2 Causes Dominant Demyelinating Charcot-Marie-Tooth Neuropathy. [electronic resource] by Hong, Young Bin Joo, Jaesoon Hyun, Young Se Kwak, Geon Choi, Yu-Ri Yeo, Ha Kyung Jwa, Dong Hwan Kim, Eun Ja Mo, Won Min Nam, Soo Hyun Kim, Sung Min Yoo, Jeong Hyun Koo, Heasoo Park, Hwan Tae Chung, Ki Wha Choi, Byung-Ok Producer: 20160719 In: PLoS genetics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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