Wikidata

(Q24322938)

English

Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B

scientific article

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Statements

title
Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B (English)
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author name string
K Okumoto
series ordinal
1
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R Itoh
series ordinal
2
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N Shimozawa
series ordinal
3
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Y Suzuki
series ordinal
4
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S Tamura
series ordinal
5
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N Kondo
series ordinal
6
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Y Fujiki
series ordinal
7
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publication date
September 1998
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volume
7
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page(s)
1399-405
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issue
9
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Identifiers

DOI
10.1093/HMG/7.9.1399
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PubMed ID
9700193
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