Genetic heterogeneity in acatalasemia

Electrophoresis

Volumn 17, Issue 8, 1996, Pages 1302-1303

  Góth, László ^a   Páy, Anikó ^b  

^a UNIVERSITY OF DEBRECEN   (Hungary)

^b INSTITUTE OF EXPERIMENTAL MEDICINE   (Hungary)

Author keywords

G to A splicing mutation; Heteroduplex; Hungarian acatalasemia; Nucleotide sequence; Single strand conformational polymorphism

Indexed keywords

NUCLEOTIDES;

G TO A SPLICING MUTATION; GENETIC HETEROGENEITIES; HETERODUPLEX; HUNGARIAN ACATALASEMIA; HUNGARIANS; LONG PRODUCTS; NUCLEOTIDE SEQUENCING; NUCLEOTIDES SEQUENCES; SEQUENCE ANALYSIS; SINGLE STRAND CONFORMATIONAL POLYMORPHISM;

POLYMERASE CHAIN REACTION;

ARTICLE; CATALASE DEFICIENCY; GENETIC HETEROGENEITY; HUMAN; NUCLEOTIDE SEQUENCE; POINT MUTATION; POLYMERASE CHAIN REACTION;

EID: 0029846912     PISSN: 01730835     EISSN: None     Source Type: Journal    
DOI: 10.1002/elps.1150170805     Document Type: Article

References (13)

1. Takahara, S., Miyamoto, H. J., J. Othorhin. Soc. Jpn. 1948, 51, 163-164.
2. Aebi, H., Heiniger, J. P., Butler, R., Hassig, A., Experientia 1961, 17, 466.
3. Quan, F., Korneluk, R. G., Tropak, M. B., Gravel, R. A., Nucleic Acids Res. 1986, 14, 5321-5335.
4. Crawford, D. R., Mirault, M. E., Moret, R., Zbinden, I., Cerutti, P. A., Biochem. Biophys. Res. Comm. 1988, 153, 59-66.
5. Aebi, H., Bossi, E., Cantz, M., Matsubara, S., Suter, H., in: Beutler, E. (Ed.), Hereditary Disorders of Erythrocyte Metabolism, Vol. 1, Grune and Stratton, New York 1968, pp. 41-65.
6. Ogata, M., Satoh, Y., Electrophoresis 1988, 9, 128-131.
7. Ogata, M., Suzuki, K., Satoh, Y., Electrophoresis 1989, 10, 194-198.
8. Wen, J. K., Osumi, T., Hashimoto, T., Ogata, M., J. Mol. Biol. 1990, 211, 383-393.
9. Kishimoto, Y., Murakami, Y., Hayashi, K., Takahara, S., Sugimura, T., Sekiya, T., Hum. Genet. 1992, 88, 487-490.
10. Ogata, M., Hum. Genet. 1991, 86, 331-340.
11. Góth, L., Clin. Chim. Acta 1992, 207, 155-158.
12. Góth, L., Enzyme 1992, 46, 252-258.
13. Góth, L., Vitai, M., Clin. Chim. Acta 1995, 233, 75-79.