Literature DB >> 5420794

Cystathioninemia: a benign genetic condition.

C R Scott, S W Dassell, S H Clark, C Chiang-Teng, K R Swedberg.   

Abstract

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Year:  1970        PMID： 5420794     DOI： 10.1016/s0022-3476(70)80407-3

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


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  5 in total

1.  Cystathionase deficiency in fibroblast cultures from a patient with primary cystathioninuria.

Authors:  A H Bittles; N A Carson
Journal:  J Med Genet       Date:  1974-06       Impact factor: 6.318

2.  Homocystinuria due to cystathionine synthase deficiency. Studies of nitrogen balance and sulfur excretion.

Authors:  J R Poole; S H Mudd; E B Conerly; W A Edwards
Journal:  J Clin Invest       Date:  1975-05       Impact factor: 14.808

3.  Genomic basis of cystathioninuria (MIM 219500) revealed by multiple mutations in cystathionine gamma-lyase (CTH).

Authors:  Jian Wang; Robert A Hegele
Journal:  Hum Genet       Date:  2003-02-06       Impact factor: 4.132

Review 4.  Chemical Biology of H2S Signaling through Persulfidation.

Authors:  Milos R Filipovic; Jasmina Zivanovic; Beatriz Alvarez; Ruma Banerjee
Journal:  Chem Rev       Date:  2017-11-07       Impact factor: 60.622

5.  Inborn errors of metabolism. Vitamin-responsive genetic disease.

Authors:  S H Mudd
Journal:  J Clin Pathol Suppl (R Coll Pathol)       Date:  1974
  5 in total

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