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Article

Localization of the Gene for Thiamine-Responsive Megaloblastic Anemia Syndrome, on the Long Arm of Chromosome 1, by Homozygosity Mapping

1 Dec 1997

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Share to Alcoholism and Thiamine Deficiency
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 9399900
DOI: 10.1086/301642

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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Localization of the Gene for Thiamine-Responsive Megaloblastic Anemia Syndrome, on the Long Arm of Chromosome 1, by Homozygosity MappingPMID 9399900Read ↗

Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness.Semantic proximity Read ↗

Thiamine-responsive megaloblastic anemia syndrome: a disorder of high-affinity thiamine transport.Semantic proximity Read ↗

The gene mutated in thiamine-responsive anaemia with diabetes and deafness (TRMA) encodes a functional thiamine transporter.Semantic proximity Read ↗

Homozygosity and Linkage-Disequilibrium Mapping of the Syndrome of Congenital Hypoparathyroidism, Growth and Mental Retardation, and Dysmorphism to a 1-cM Interval on Chromosome 1q42-43Semantic proximity Read ↗

Mutations in a new gene encoding a thiamine transporter cause thiamine-responsive megaloblastic anaemia syndrome.Semantic proximity Read ↗

Linkage of pycnodysostosis to chromosome 1q21 by homozygosity mappingSemantic proximity Read ↗

Cloning of the Human Thiamine Transporter, a Member of the Folate Transporter FamilySemantic proximity Read ↗

Defective high-affinity thiamine transporter leads to cell death in thiamine-responsive megaloblastic anemia syndrome fibroblasts.Semantic proximity Read ↗

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