Localization of the gene for thiamine-responsive megaloblastic anemia syndrome, on the long arm of chromosome 1, by homozygosity mapping.

Thiamine-responsive megaloblastic anemia, also known as "TRMA" or "Rogers syndrome," is an early-onset autosomal recessive disorder defined by the occurrence of megaloblastic anemia, diabetes mellitus, and sensorineural deafness, responding in varying degrees to thiamine treatmen...

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Detalhes bibliográficos
Main Authors: Neufeld, E J, Mandel, H, Raz, T, Szargel, R, Yandava, C N, Stagg, A, Fauré, S, Barrett, T, Buist, N, Cohen, N
Formato: Artigo
Idioma:Inglês
Publicado em: 1997
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1716091/
https://ncbi.nlm.nih.gov/pubmed/9399900
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