Literature DB >> 2795358

False positive results from the alanine loading test for ornithine carbamoyltransferase deficiency heterozygosity.

A E MacKenzie1, H L MacLeod, H M Heick, R G Korneluk.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1989        PMID： 2795358     DOI： 10.1016/s0022-3476(89)80294-x

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


× No keyword cloud information.
  3 in total

Review 1.  Inherited metabolic diseases affecting the carrier.

Authors:  W Endres
Journal:  J Inherit Metab Dis       Date:  1997-03       Impact factor: 4.982

2.  Single-strand conformational polymorphism and direct sequencing applied to carrier testing in families with ornithine transcarbamylase deficiency.

Authors:  M Y Tsai; R A Holzknecht; M Tuchman
Journal:  Hum Genet       Date:  1993-05       Impact factor: 4.132

3.  How reliable is the allopurinol load in detecting carriers for ornithine transcarbamylase deficiency?

Authors:  S Grünewald; L Fairbanks; S Genet; T Cranston; J Hüsing; J V Leonard; M P Champion
Journal:  J Inherit Metab Dis       Date:  2004       Impact factor: 4.982
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.