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Literature DB >> 13904105

The frequency in Japan of carriers of the rare "recessive" gene causing acatalasemia.

H B HAMILTON, J V NEEL, T Y KOBARA, K OZAKI.

Abstract

Entities: Disease Gene

Keywords: CATALASE/blood

Mesh：

Substances：
Catalase

Year: 1961 PMID： 13904105 PMCID： PMC290929 DOI： 10.1172/JCI104446

Source DB: PubMed Journal: J Clin Invest ISSN： 0021-9738 Impact factor: 14.808

× No keyword cloud information.

9 in total

1. Hypocatalasemia: a new genetic carrier state.

Authors: S TAKAHARA; H B HAMILTON; J V NEEL; T Y KOBARA; Y OGURA; E T NISHIMURA
Journal: J Clin Invest Date: 1960-04 Impact factor: 14.808

2. Carrier state in human acatalasemia.

Authors: E T NISHIMURA; H B HAMILTON; T Y KOBARA; S TAKAHARA; Y OGURA; K DOI
Journal: Science Date: 1959-08-07 Impact factor: 47.728

3. A note on deaf mutism.

Authors: C S CHUNG; O W ROBINSON; N E MORTON
Journal: Ann Hum Genet Date: 1959-12 Impact factor: 1.670

4. The mutational load due to detrimental genes in man.

Authors: N E MORTON
Journal: Am J Hum Genet Date: 1960-09 Impact factor: 11.025

5. Empirical risks in consanguineous marriages: sex ratio, malformation, and viability.

Authors: W J SCHULL
Journal: Am J Hum Genet Date: 1958-09 Impact factor: 11.025

6. Hereditary deaf mutism, with particular reference to Northern Ireland.

Authors: A C STEVENSON; E A CHEESEMAN
Journal: Ann Hum Genet Date: 1956-02 Impact factor: 1.670

7. The Effects of Isolates on the Frequency of a Rare Human Gene.

Authors: L C Dunn
Journal: Proc Natl Acad Sci U S A Date: 1947-12 Impact factor: 11.205

8. AN ESTIMATE OF THE MUTATIONAL DAMAGE IN MAN FROM DATA ON CONSANGUINEOUS MARRIAGES.

Authors: N E Morton; J F Crow; H J Muller
Journal: Proc Natl Acad Sci U S A Date: 1956-11 Impact factor: 11.205

9. The incidence of consanguineous matings in Japan, with remarks on the estimation of comparative gene frequencies and the expected rate of appearance of induced recessive mutations.

Authors: J V Neel; M Kodani; R Brewer; R C Anderson
Journal: Am J Hum Genet Date: 1949-12 Impact factor: 11.025

9 in total

11 in total

The frequency in Japan of carriers of the rare "recessive" gene causing acatalasemia.

1. Hypocatalasemia: a new genetic carrier state.

2. Carrier state in human acatalasemia.

3. A note on deaf mutism.

4. The mutational load due to detrimental genes in man.

5. Empirical risks in consanguineous marriages: sex ratio, malformation, and viability.

6. Hereditary deaf mutism, with particular reference to Northern Ireland.

7. The Effects of Isolates on the Frequency of a Rare Human Gene.

8. AN ESTIMATE OF THE MUTATIONAL DAMAGE IN MAN FROM DATA ON CONSANGUINEOUS MARRIAGES.

9. The incidence of consanguineous matings in Japan, with remarks on the estimation of comparative gene frequencies and the expected rate of appearance of induced recessive mutations.

1. GENETIC HETEROGENEITY IN HUMAN ACATALASIA.

2. BLOOD GROUP FREQUENCIES IN MONGOLS.

3. Frequency of hypocatalasemia in a sample of Spanish population.

4. Acatalasia was omitted.

5. Imbalance of blood group A subtypes and the existence of superactive B gene in Japanese in Hiroshima and Nagasaki.

6. The effects of parental consanguinity and inbreeding in Hirado, Japan. V. Summary and interpretation.

7. Haemoglobin and red cell enzyme changes in juvenile myeloid leukaemia.

8. Further studies on the Xavante Indians. X. Some hypotheses-generalizations resulting from these studies.

9. The frequency among Japanese of heterozygotes for deficiency variants of 11 enzymes.

10. Frequency of enzyme deficiency variants in erythrocytes of newborn infants.