Literature DB >> 4623258

Sarcosine dehydrogenase deficiency, the enzyme defect in hypersarcosinemia.

T Gerritsen.   

Abstract

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Year:  1972        PMID： 4623258

Source DB:  PubMed          Journal:  Helv Paediatr Acta        ISSN： 0018-022X


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  5 in total

1.  Hypersarcosinemia with craniostenosis-syndactylism syndrome.

Authors:  R Minami; K Olek; P Wardenbach
Journal:  Humangenetik       Date:  1975-06-19

2.  Cloning of dimethylglycine dehydrogenase and a new human inborn error of metabolism, dimethylglycine dehydrogenase deficiency.

Authors:  B A Binzak; R A Wevers; S H Moolenaar; Y M Lee; W L Hwu; J Poggi-Bach; U F Engelke; H M Hoard; J G Vockley; J Vockley
Journal:  Am J Hum Genet       Date:  2001-02-28       Impact factor: 11.025

3.  Sarcosinaemia in a patient with Usher syndrome.

Authors:  E Christensen; N J Brandt; T Rosenberg
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

4.  Mutations in the sarcosine dehydrogenase gene in patients with sarcosinemia.

Authors:  Ifat Bar-joseph; Elon Pras; Haike Reznik-Wolf; Dina Marek-Yagel; Almogit Abu-Horvitz; Maya Dushnitzky; Nurit Goldstein; Shlomit Rienstein; Michal Dekel; Ben Pode-Shakked; Joseph Zlotnik; Anelia Benarrosh; Philippe Gillery; Niklaus Hofliger; Christiane Auray-Blais; Roselyne Garnotel; Yair Anikster
Journal:  Hum Genet       Date:  2012-07-24       Impact factor: 4.132

5.  Variability in the phenotypic expression of abnormal sarcosine metabolism in a family.

Authors:  E S Kang; J Seyer; T A Todd; C Herrera
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132
  5 in total

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