|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
10
|
|
pubmed:dateCreated |
1993-11-2
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|
pubmed:abstractText |
Dermatosparaxis is an autosomal recessive connective tissue disorder in animals that is caused by abnormal processing of type I procollagen and results in skin laxity and fragility. Only three humans with characteristic biochemical and electronmicroscopic findings have been recognized to date.
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pubmed:grant |
|
|
pubmed:commentsCorrections |
|
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pubmed:language |
eng
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|
pubmed:journal |
|
|
pubmed:citationSubset |
AIM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Oct
|
|
pubmed:issn |
0003-987X
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pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
129
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
1310-5
|
|
pubmed:dateRevised |
2008-3-17
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|
pubmed:meshHeading |
|
|
pubmed:year |
1993
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|
pubmed:articleTitle |
Dermatosparaxis in children. A case report and review of the newly recognized phenotype.
|
|
pubmed:affiliation |
Department of Genetics, Yale University School of Medicine, New Haven, Conn.
|
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Case Reports
|
