Wikidata

(Q55670897)

English

Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination

article by L E Warner et al published September 1996 in Neuron

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Statements

title
Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination (English)
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author name string
L E Warner
series ordinal
1
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M J Hilz
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2
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S H Appel
series ordinal
3
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J M Killian
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4
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E H Kolodry
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5
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G Karpati
series ordinal
6
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S Carpenter
series ordinal
7
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G V Watters
series ordinal
8
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C Wheeler
series ordinal
9
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D Witt
series ordinal
10
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A Bodell
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11
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E Nelis
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12
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C Van Broeckhoven
series ordinal
13
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J R Lupski
series ordinal
14
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publication date
September 1996
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published in
Neuron
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volume
17
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issue
3
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page(s)
451-60
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Identifiers

PubMed ID
8816708
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