Abstract
Charcot‐Marie‐Tooth type 1B neuropathy: A mutation at the single glycosylation site in the major peripheral myelin glycoprotein P0
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https://doi.org/10.1002/(sici)1098-1004(1996)8:2<185::aid-humu13>3.3.co;2-3
Journal: Human Mutation | Publication Date: Jan 1, 1996 |
Charcot‐Marie‐Tooth type 1B neuropathy: A mutation at the single glycosylation site in the major peripheral myelin glycoprotein P0
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