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rdf:type |
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|
lifeskim:mentions |
|
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pubmed:issue |
4
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pubmed:dateCreated |
1983-1-19
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|
pubmed:abstractText |
An uncommon abnormal hemoglobin, Hb Belfast (beta 15 Trp replaced by Arg) was discovered in a patient of Italian origin. The patient was a 42-year-old man who developed two episodes of jaundice after a prolonged administration of an antituberculous drugs. Family studies revealed that several members were asymptomatic carriers of Hb Belfast.
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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:issn |
0363-0269
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pubmed:author |
|
|
pubmed:issnType |
Print
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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 |
391-6
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:7141875-Adult,
pubmed-meshheading:7141875-Arginine,
pubmed-meshheading:7141875-Chemical Phenomena,
pubmed-meshheading:7141875-Chemistry,
pubmed-meshheading:7141875-Female,
pubmed-meshheading:7141875-Hemoglobins,
pubmed-meshheading:7141875-Hemoglobins, Abnormal,
pubmed-meshheading:7141875-Humans,
pubmed-meshheading:7141875-Italy,
pubmed-meshheading:7141875-Male,
pubmed-meshheading:7141875-Pedigree,
pubmed-meshheading:7141875-Tryptophan
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|
pubmed:year |
1982
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|
pubmed:articleTitle |
Hb Belfast (beta 15 Trp replaced by Arg) in an Italian family.
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|
pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
|
