(Q33735640)
Statements
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Hereditary neuropathy with liability to pressure palsies with a partial deletion of the region often duplicated in Charcot-Marie-Tooth disease, type 1A. (English)
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Van Broeckhoven C
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Chapon F
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Diraison P
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Lechevalier B
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Chazot G
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Viader F
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Bonnebouche C
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Vandenberghe A
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Timmerman V
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Vandenberghe A
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1 November 1996
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535-536
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Identifiers
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