(Q33585460)

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Homocystinuria: an observation on the inheritance of cystathionine synthase deficiency

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PubMed publication ID

5971056

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28 July 2017

title

Homocystinuria: an observation on the inheritance of cystathionine synthase deficiency (English)

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Europe PubMed Central

PubMed publication ID

28 July 2017

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Gaull G

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Europe PubMed Central

PubMed publication ID

5971056

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28 July 2017

Gaitonde MK

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PubMed publication ID

5971056

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28 July 2017

language of work or name

English

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publication date

1 September 1966

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PubMed publication ID

5971056

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28 July 2017

published in

Journal of Medical Genetics

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PubMed publication ID

28 July 2017

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Europe PubMed Central

PubMed publication ID

28 July 2017

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Europe PubMed Central

PubMed publication ID

5971056

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28 July 2017

page(s)

194-197

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Europe PubMed Central

PubMed publication ID

5971056

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28 July 2017

cites work

HOMOCYSTINURIA: AN ENZYMATIC DEFECT.

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012938

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21 June 2018

HOMOCYSTINURIA. BIOCHEMICAL STUDIES OF TISSUES INCLUDING A COMPARISON WITH CYSTATHIONINURIA

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012938

retrieved

31 October 2018

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

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/5971056

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12 December 2020

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1 reference

Europe PubMed Central

PubMed publication ID

5971056

retrieved

28 July 2017

PubMed publication ID

5971056

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5971056

retrieved

28 July 2017

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