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14158292
Source:
http://linkedlifedata.com/resource/pubmed/id/14158292
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Subject
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Context
pubmed-article:14158292
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lifeskim:mentions
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pubmed-article:14158292
pubmed:dateCreated
1964-10-1
lld:pubmed
pubmed-article:14158292
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pubmed-article:14158292
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ger
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pubmed:citationSubset
OM
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pubmed-article:14158292
pubmed:status
MEDLINE
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pubmed-article:14158292
pubmed:month
Feb
lld:pubmed
pubmed-article:14158292
pubmed:issn
0367-004X
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pubmed-article:14158292
pubmed:author
pubmed-author:WEWALKAFF
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pubmed-article:14158292
pubmed:author
pubmed-author:SCHOBERHH
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pubmed:author
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pubmed-article:14158292
pubmed:issnType
Print
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pubmed-article:14158292
pubmed:day
21
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pubmed-article:14158292
pubmed:volume
185
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pubmed-article:14158292
pubmed:owner
NLM
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pubmed-article:14158292
pubmed:authorsComplete
Y
lld:pubmed
pubmed-article:14158292
pubmed:pagination
579-97
lld:pubmed
pubmed-article:14158292
pubmed:dateRevised
2011-11-17
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pubmed-article:14158292
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pubmed-article:14158292
pubmed:year
1964
lld:pubmed
pubmed-article:14158292
pubmed:articleTitle
[ON A FAMILIAL DISEASE WITH AN UNUSUAL NEUROLOGIC SYMPTOM COMBINATION, OLIGOPHRENIA, DEMENTIA, MULTIPLE SKIN ULCERATIONS, SPLENOMEGALY AND AMINO ACID METABOLIC DISORDERS].
lld:pubmed
pubmed-article:14158292
pubmed:publicationType
Journal Article
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