Dihydropyrimidinase Deficiency: Structural Organization, Chromosomal Localization, and Mutation Analysis of the Human Dihydropyrimidinase Gene-Reference-Cited by-同舟云学术

Dihydropyrimidinase Deficiency: Structural Organization, Chromosomal Localization, and Mutation Analysis of the Human Dihydropyrimidinase Gene

Published:1998-09 Issue:3 Volume:63 Page:717-726
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Hamajima Naoki,Kouwaki Masanori,Vreken Peter,Matsuda Kouichi,Sumi Satoshi,Imaeda Masayuki,Ohba Satoru,Kidouchi Kiyoshi,Nonaka Masaru,Sasaki Makoto,Tamaki Nanaya,Endo Yuichi,De Abreu Ronnie,Rotteveel Jan,van Kuilenburg André,van Gennip Albert,Togari Hajime,Wada Yoshiro

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference32 articles.

1. Dihydropyrimidinase deficiency and congenital microvillous atrophy;Assmann;J Inherit Metab Dis,1997

2. Bovine liver dihydropyrimidine amidohydrolase: purification, properties, and characterization as a zinc metalloenzyme;Brooks;Arch Biochem Biophys,1983

3. Dihydropyrimidine amidohydrolase is a zinc metalloenzyme;Brooks;Biochim Biophys Acta,1979

4. Apparent cleidocranial dysplasia with abnormalities of 8q22 in three individuals;Brueton;Am J Med Genet,1992

5. Dihydropyrimidinuria;Duran;Lancet,1990

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