Literature DB >> 5971056

Homocystinuria: an observation on the inheritance of cystathionine synthase deficiency.

G Gaull, M K Gaitonde.   

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Year:  1966        PMID: 5971056      PMCID: PMC1012938          DOI: 10.1136/jmg.3.3.194

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


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  3 in total

1.  HOMOCYSTINURIA. BIOCHEMICAL STUDIES OF TISSUES INCLUDING A COMPARISON WITH CYSTATHIONINURIA.

Authors:  D P BRENTON; D C CUSWORTH; G E GAULL
Journal:  Pediatrics       Date:  1965-01       Impact factor: 7.124

2.  HOMOCYSTINURIA: AN ENZYMATIC DEFECT.

Authors:  S H MUDD; J D FINKELSTEIN; F IRREVERRE; L LASTER
Journal:  Science       Date:  1964-03-27       Impact factor: 47.728

3.  [Incorporation and degradation of methionine by crystalline lens of bovides].

Authors:  P MANDEL; U DARDENNE; A LESSINGER
Journal:  C R Hebd Seances Acad Sci       Date:  1957-09-09
  3 in total
  3 in total

Review 1.  The skin in genetically-controlled metabolic disorders.

Authors:  P C Newbold
Journal:  J Med Genet       Date:  1973-06       Impact factor: 6.318

2.  Pupil-block glaucoma in homocystinuria.

Authors:  S S Johnston
Journal:  Br J Ophthalmol       Date:  1968-03       Impact factor: 4.638

3.  A study of the sulphur amino acids of rat tissues.

Authors:  G E Gaull; M K Gaitonde
Journal:  Biochem J       Date:  1967-01       Impact factor: 3.857

  3 in total

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