Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1988-7-22
pubmed:databankReference
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/J00093, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/J00094, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/J00096, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/J00158, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/J00159, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/J00160, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/J00161, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/J00162, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/J00163, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/J00164, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/J00165, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/J00166, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/J00167, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/J00168, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/J00169, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/J00170, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/J00171, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/J00172, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/J00173, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/J00174, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/J00175, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/J00177, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/J00178, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/J00179, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/K01239, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/K01890, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/K02544, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M18047, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M19067, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X00423
pubmed:abstractText
Sequence analyses of amplified DNA from a Yugoslavian patient with Hb Lepore-beta-thalassemia and from his father with a simple beta-thalassemia trait have revealed a T----A mutation within the ATA box at a position 30 base pairs upstream from the Cap site. The nucleotide substitution was confirmed through dot-blot analysis of amplified DNA with specific 32P-labeled synthetic oligonucleotide probes. The patient had a clinically severe condition; his Hb Lepore-beta-thalassemia was of the beta + type, as about 8-10% of the non-alpha chain was normal beta A. The same T----A mutation at nucleotide -30 was present on both chromosomes of a young Turkish patient who suffered from a thalassemia intermedia with a low level of Hb F (13.1%) and a relatively high beta A chain synthesis. These data are similar to those obtained for other types of beta +-thalassemia caused by comparable substitutions at positions 31, 29, and 28 base pairs upstream from the Cap site of the beta-globin gene.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0006-291X
pubmed:author
pubmed:issnType
Print
pubmed:day
16
pubmed:volume
153
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
741-7
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed:year
1988
pubmed:articleTitle
Beta-thalassemia due to a T----A mutation within the ATA box.
pubmed:affiliation
Department of Cell and Molecular Biology, Medical College of Georgia, Augusta 30912-2100.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, U.S. Gov't, Non-P.H.S., Research Support, Non-U.S. Gov't