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Hum Mutat. 1996;8(2):185-6.

Charcot-Marie-Tooth type 1B neuropathy: a mutation at the single glycosylation site in the major peripheral myelin glycoprotein Po.

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1
Laboratoire de Neurogénétique Moléculaire, URA 1488 CNRS, Université de Paris VI, France.

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