(Q28306153)

1

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A Sahota

2

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U Gresser

3

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J Chen

4

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P J Stambrook

5

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J A Tischfield

6

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N Zöllner

Polymerase chain reaction amplification and sequence analysis of human mutant adenine phosphoribosyltransferase genes: the nature and frequency of errors caused by Taq DNA polymerase

7

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language of work or name

English

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publication date

30 December 1990

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published in

Klinische Wochenschrift

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volume

69

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issue

24

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page(s)

1152-5

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cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF01815434

Sph I restriction fragment length polymorphism on human chromosome 16 detected with an APRT gene probe

21 January 2018

1 reference

12 December 2020

Restriction fragment length polymorphisms of HPRT and APRT genes in Japanese population.

1 reference

12 December 2020

Cloning of a functional human adenine phosphoribosyltransferase (APRT) gene: Identification of a restriction fragment length polymorphism and preliminary analysis of DNAs from APRT-deficient families and cell mutants

1 reference

12 December 2020

Nephrolithiasis in twins with APRT-deficiency. Stones as a marker of an inborn error of metabolism

1 reference

12 December 2020

2,8-dihydroxyadenine urinary calculus: the significance of exact physical calculus analysis

1 reference

12 December 2020

Crossovers within a short DNA sequence indicate a long evolutionary history of the APRT*J mutation

1 reference

12 December 2020

Human adenine phosphoribosyltransferase deficiency. Demonstration of a single mutant allele common to the Japanese

1 reference

12 December 2020

New diagnostic and therapeutic aspects of 2,8-dihydroxyadenine lithiasis. Another case of complete adenine phosphoribosyltransferase deficiency

1 reference

12 December 2020

2,8-Dihydroxyadeninuria: laboratory diagnosis and therapy control

1 reference

12 December 2020

Splicing mutations in the CHO DHFR gene preferentially induced by (+/-)-3 alpha,4 beta-dihydroxy-1 alpha,2 alpha-epoxy-1,2,3,4- tetrahydrobenzo[c]phenanthrene

1 reference

12 December 2020

Human adenine phosphoribosyltransferase. Identification of allelic mutations at the nucleotide level as a cause of complete deficiency of the enzyme

1 reference

12 December 2020

HCC ligation: rapid and specific DNA construction with blunt ended DNA fragments

1 reference

12 December 2020