Matches in SemOpenAlex for { <https://semopenalex.org/work/W3202202237> ?p ?o ?g. }
Showing items 1 to 61 of
61
with 100 items per page.
- W3202202237 endingPage "128" @default.
- W3202202237 startingPage "124" @default.
- W3202202237 abstract "β-thalassemia is an inherited blood disorder that is the most common single-gene disorder worldwide and in Vietnam. This study reports an intermedia β thalassemia patient in a family from Northern Vietnam. The mother has compound heterozygous thalassemia presenting mutation of hemoglobin HBB: c.79G>A associated with HBB: c.-78A>G. The result indicates that the determination of molecular characterization of subjects presenting normal HbA2 level associated with abnormal red cell indices is needed for accurate diagnosis and improved genetic counseling." @default.
- W3202202237 created "2021-10-11" @default.
- W3202202237 creator A5043407440 @default.
- W3202202237 date "2021-06-10" @default.
- W3202202237 modified "2023-10-14" @default.
- W3202202237 title "A Compound Heterozygous HBB: C.79G>A Associated with HBB: C.-78A>G Mutation of HBB Gene Leading to Β-Thalassemia Intermedia in A Vietnamese Patient: A Case Study" @default.
- W3202202237 doi "https://doi.org/10.34297/ajbsr.2021.13.001842" @default.
- W3202202237 hasPublicationYear "2021" @default.
- W3202202237 type Work @default.
- W3202202237 sameAs 3202202237 @default.
- W3202202237 citedByCount "0" @default.
- W3202202237 crossrefType "journal-article" @default.
- W3202202237 hasAuthorship W3202202237A5043407440 @default.
- W3202202237 hasBestOaLocation W32022022371 @default.
- W3202202237 hasConcept C103621254 @default.
- W3202202237 hasConcept C104317684 @default.
- W3202202237 hasConcept C12125453 @default.
- W3202202237 hasConcept C138885662 @default.
- W3202202237 hasConcept C203014093 @default.
- W3202202237 hasConcept C2776175824 @default.
- W3202202237 hasConcept C2777799968 @default.
- W3202202237 hasConcept C2779668550 @default.
- W3202202237 hasConcept C2994225774 @default.
- W3202202237 hasConcept C41895202 @default.
- W3202202237 hasConcept C501734568 @default.
- W3202202237 hasConcept C54355233 @default.
- W3202202237 hasConcept C86803240 @default.
- W3202202237 hasConceptScore W3202202237C103621254 @default.
- W3202202237 hasConceptScore W3202202237C104317684 @default.
- W3202202237 hasConceptScore W3202202237C12125453 @default.
- W3202202237 hasConceptScore W3202202237C138885662 @default.
- W3202202237 hasConceptScore W3202202237C203014093 @default.
- W3202202237 hasConceptScore W3202202237C2776175824 @default.
- W3202202237 hasConceptScore W3202202237C2777799968 @default.
- W3202202237 hasConceptScore W3202202237C2779668550 @default.
- W3202202237 hasConceptScore W3202202237C2994225774 @default.
- W3202202237 hasConceptScore W3202202237C41895202 @default.
- W3202202237 hasConceptScore W3202202237C501734568 @default.
- W3202202237 hasConceptScore W3202202237C54355233 @default.
- W3202202237 hasConceptScore W3202202237C86803240 @default.
- W3202202237 hasIssue "1" @default.
- W3202202237 hasLocation W32022022371 @default.
- W3202202237 hasOpenAccess W3202202237 @default.
- W3202202237 hasPrimaryLocation W32022022371 @default.
- W3202202237 hasRelatedWork W1969512347 @default.
- W3202202237 hasRelatedWork W2014379101 @default.
- W3202202237 hasRelatedWork W2023079987 @default.
- W3202202237 hasRelatedWork W2034719394 @default.
- W3202202237 hasRelatedWork W2062123316 @default.
- W3202202237 hasRelatedWork W2072962785 @default.
- W3202202237 hasRelatedWork W2093286327 @default.
- W3202202237 hasRelatedWork W2146367389 @default.
- W3202202237 hasRelatedWork W2963449606 @default.
- W3202202237 hasRelatedWork W3165561447 @default.
- W3202202237 hasVolume "13" @default.
- W3202202237 isParatext "false" @default.
- W3202202237 isRetracted "false" @default.
- W3202202237 magId "3202202237" @default.
- W3202202237 workType "article" @default.