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Niemann-Pick disease in association with homozygous hemoglobin E: A case report

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dc.contributor.authorV. S. Tanphaichitren_US
dc.contributor.authorV. Suvatteen_US
dc.contributor.authorS. Tuchindaen_US
dc.contributor.authorC. Mahasandanaen_US
dc.contributor.authorD. A. Wengeren_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-06-01T06:30:40Z
dc.date.available2018-06-01T06:30:40Z
dc.date.issued1979-12-01en_US
dc.description.abstractThe first case of Niemann-Pick disease Type A in a Thai infant was reported. The patient also had abnormal hemoglobin E. The diagnosis was based on the clinical features, bone marrow findings and sphingomyelinase levels in the culture of skin fibroblasts. The autosomal recessive mode of inheritance was confirmed in this case.en_US
dc.identifier.citationSoutheast Asian Journal of Tropical Medicine and Public Health. Vol.10, No.4 (1979), 562-567en_US
dc.identifier.issn00383619en_US
dc.identifier.other2-s2.0-0018632493en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/13227
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0018632493&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleNiemann-Pick disease in association with homozygous hemoglobin E: A case reporten_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0018632493&origin=inwarden_US

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