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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
10
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pubmed:dateCreated |
2008-10-8
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pubmed:abstractText |
We studied 24 Hungarian patients from 23 unrelated families to identify the genetic background of the entire type 3 von Willebrand disease (VWD) population in this country. The current report focuses on the molecular characterization of a novel large deletion.
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pubmed:commentsCorrections |
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pubmed:language |
eng
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pubmed:journal |
|
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pubmed:citationSubset |
IM
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pubmed:chemical |
|
|
pubmed:status |
MEDLINE
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|
pubmed:month |
Oct
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|
pubmed:issn |
1538-7836
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pubmed:author |
|
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pubmed:issnType |
Electronic
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pubmed:volume |
6
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1729-35
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:18665926-5' Flanking Region,
pubmed-meshheading:18665926-Alu Elements,
pubmed-meshheading:18665926-Exons,
pubmed-meshheading:18665926-Family,
pubmed-meshheading:18665926-Founder Effect,
pubmed-meshheading:18665926-Gene Deletion,
pubmed-meshheading:18665926-Gene Frequency,
pubmed-meshheading:18665926-Humans,
pubmed-meshheading:18665926-Hungary,
pubmed-meshheading:18665926-Introns,
pubmed-meshheading:18665926-von Willebrand Diseases,
pubmed-meshheading:18665926-von Willebrand Factor
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pubmed:year |
2008
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pubmed:articleTitle |
An Alu-mediated novel large deletion is the most frequent cause of type 3 von Willebrand disease in Hungary.
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pubmed:affiliation |
Semmelweis Medical University, Central Laboratory of Immunology and Haematology, Budapest, Hungary. adrienn.mohl@yahoo.com
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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