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Article

Fetal hemoglobin and alpha thalassemia modulate the phenotypic expression of HbSD-Punjab.

International journal of laboratory hematology - 1 Aug 2014

Patel D K, Purohit P, Dehury S, Das P, Dutta A, Meher S, Patel S, Bag S, Mashon R S, Das K

Abstract excerpt

INTRODUCTION: HbSD-Punjab (HbSD) is a less common form of sickle cell disease (SCD) and discrimination between HbSD and HbSS is not possible on alkaline electrophoresis because the two variants overlap in the compound heterozygous state. There are only a few publications consisting mostly of case reports. Thus, the phenotypic expression of HbSD and its modifiers has not been studied. METHODS: We studied the...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 24245819
DOI: 10.1111/ijlh.12165

Genes

SCD

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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