Identification of two independent Japanese mutant ...[Adv Exp Med Biol. 1991] - PubMed Result

SearchDatabase nameforSearch term

Advanced Search

Your browser version may not work well with NCBI's Web applications. More information here...

Display Show

All: 1

Review: 0

Click to change filter selection through MyNCBI.

1: Adv Exp Med Biol. 1991;309B:121-4.Links

Identification of two independent Japanese mutant HPRT genes using the PCR technique.

Yamada Y, Goto H, Ogasawara N.

Department of Genetics, Institute for Developmental Research, Aichi, Japan.

PMID: 1840476 [PubMed - indexed for MEDLINE]

Related articles

Molecular analysis of five independent Japanese mutant genes responsible for hypoxanthine guanine phosphoribosyltransferase (HPRT) deficiency.
Hum Genet. 1992 Dec; 90(4):379-84.

[Hum Genet. 1992]
A germ line mutation within the coding sequence for the putative 5-phosphoribosyl-1-pyrophosphate binding site of hypoxanthine-guanine phosphoribosyltransferase (HPRT) in a Lesch-Nyhan patient: missense mutations within a functionally important region probably cause disease.
Hum Genet. 1992 Dec; 90(4):385-8.

[Hum Genet. 1992]
Genetic analysis of the HPRT mutation of Lesch-Nyhan syndrome in a Chinese family.
Zhonghua Yi Xue Za Zhi (Taipei). 1995 Dec; 56(6):359-66.

[Zhonghua Yi Xue Za Zhi (Taipei). 1995]
ReviewHPRT: gene structure, expression, and mutation.
Annu Rev Genet. 1985; 19:127-48.

[Annu Rev Genet. 1985]
ReviewMolecular analysis of mutation at the human hprt locus.
Acta Physiol Scand Suppl. 1990; 592:85-92.

[Acta Physiol Scand Suppl. 1990]
» See reviews... | » See all...

Recent Activity

Clear Turn Off Turn On

Identification of two independent Japanese mutant HPRT genes using the PCR technique.Identification of two independent Japanese mutant HPRT genes using the PCR technique.

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Display Show