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Article

A Novel Human Catalase Mutation (358 T_del) Causing Japanese-type Acatalasemia

1 Dec 1995

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 8673475
DOI: 10.1006/bcmd.1995.0026

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

A Novel Human Catalase Mutation (358 T_del) Causing Japanese-type AcatalasemiaPMID 8673475Read ↗

A novel catalase mutation (a G insertion in exon 2) causes the type B of the Hungarian acatalasemia.Semantic proximity Read ↗

Catalase enzyme mutations and their association with diseases.Semantic proximity Read ↗

Detection of a common mutation of the catalase gene in Japanese acatalasemic patients.Semantic proximity Read ↗

Inherited catalase deficiency: is it benign or a factor in various age related disorders?Semantic proximity Read ↗

Further acatalasemia mutations in human patients from Hungary with diabetes and microcytic anemia.Semantic proximity Read ↗

Anovel catalase mutation (a GA insertion) causes the Hungarian type of acatalasemia.Semantic proximity Read ↗

Detection of a novel familial catalase mutation (Hungarian type D) and the possible risk of inherited catalase deficiency for diabetes mellitus.Semantic proximity Read ↗

A novel catalase mutation detected by polymerase chain reaction-single strand conformation polymorphism, nucleotide sequencing, and western blot analyses is responsible for the type C of Hungarian acatalasemia.Semantic proximity Read ↗

Human catalase, its polymorphisms, regulation and changes of its activity in different diseases.Semantic proximity Read ↗

Acatalasemia and diabetes mellitus.Semantic proximity Read ↗

[Acatalasemia and type 2 diabetes mellitus].Semantic proximity Read ↗

Polymorphism of 5' of the catalase gene in Hungarian acatalasemia and hypocatalasemia.Semantic proximity Read ↗

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