Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
|
pubmed:dateCreated |
1978-4-17
|
pubmed:abstractText |
During a survey for abnormal hemoglobins in Polesine (a region north of the Po river, where beta-thalassemia is very frequent) a slow moving variant was noted in a 79-yr-old woman living in Gavello, a small town in the province of Rovigo. Structural studies demonstrated a previously undescribed amino acid substitution, beta47 Asp replaced by Gly. This new variant has been named Hb Gavello.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:issn |
0363-0269
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
1
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
771-9
|
pubmed:dateRevised |
2004-11-17
|
pubmed:meshHeading |
pubmed-meshheading:604315-Aged,
pubmed-meshheading:604315-Aspartic Acid,
pubmed-meshheading:604315-Electrophoresis, Cellulose Acetate,
pubmed-meshheading:604315-Female,
pubmed-meshheading:604315-Glycine,
pubmed-meshheading:604315-Hemoglobins, Abnormal,
pubmed-meshheading:604315-Humans,
pubmed-meshheading:604315-Italy
|
pubmed:year |
1977
|
pubmed:articleTitle |
Hemoglobin Gavello - alpha 2 beta 2 47 (CD6) Asp replaced by Gly. A new hemoglobin variant from Polesine (Italy).
|
pubmed:publicationType |
Journal Article
|