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PMID: 1303180 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

A novel C to T substitution at nucleotide 1360 of cDNA which abolishes a natural Hha I site accounts for a new G6PD deficiency gene in Chinese.

Human molecular genetics ·Vol. 1 ·No. 3 ·1992-06-00 ·Pages 205

Perng LI, Chiou SS, Liu TC, Chang JG

Abstract

暂无摘要

Related Genes

G6PD

MeSH Terms

Amino Acid Sequence Asians/genetics Base Sequence DNA/genetics Deoxyribonucleases, Type II Site-Specific Glucosephosphate Dehydrogenase/genetics Glucosephosphate Dehydrogenase Deficiency/genetics Humans Molecular Sequence Data Point Mutation

Chemicals

DNA Glucosephosphate Dehydrogenase Deoxyribonucleases, Type II Site-Specific GCGC-specific type II deoxyribonucleases

Authors & Affiliations

4 authors, click to expand affiliations / ORCID

Perng L I

Department of Molecular Medicine and Clinical Pathology, Taipei Municipal Jen-Ai Hospital, Taiwan.

Chiou S S

Liu T C

Chang J G

Article Info

Journal

Human molecular genetics

Abbr.

Hum Mol Genet

ISSN

0964-6906

DOI

10.1093/hmg/1.3.205

Published

1992-06-00

Pages

205

Language

English

Region

England

NLM ID

9208958

Subset

External Links

PubMed source DOI: 10.1093/hmg/1.3.205 View journal details

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A novel C to T substitution at nucleotide 1360 of cDNA which abolishes a natural Hha I site accounts for a new G6PD deficiency gene in Chinese.

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