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Autor:
Hyun Hwang, Hyun Myung Doo, Ho S Yu, Jung M Lee, Dong W Song, Young Bin Hong, Seokjoong Kim, Jae Young Lee, Ji-Su Lee, Hee K Kim, Hee S Bae, Byung-Ok Choi, Kyu Joon Lee, Geon Kwak, Daesik Kim
Publikováno v:
Nucleic Acids Research
Charcot-Marie-Tooth 1A (CMT1A) is the most common inherited neuropathy without a known therapy, which is caused by a 1.4 Mb duplication on human chromosome 17, which includes the gene encoding the peripheral myelin protein of 22 kDa (PMP22). Overexpr