(Q30413499)

21 August 2017

Failure to demonstrate mutations affecting protein structure or function in children with congenital defects or born prematurely (English)

1 reference

21 August 2017

0 references

Neel JV

1

1 reference

PMCID

391733

21 August 2017

Mohrenweiser HW

series ordinal

2

1 reference

PMCID

391733

21 August 2017

language of work or name

English

0 references

publication date

1 September 1984

1 reference

Proceedings of the National Academy of Sciences of the United States of America

21 August 2017

5

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

21 August 2017

81

1 reference

21 August 2017

17

1 reference

21 August 2017

5499-5503

1 reference

Frequency of enzyme deficiency variants in erythrocytes of newborn infants

21 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=391733

Rate of spontaneous mutation at human loci encoding protein structure

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=391733

Search for mutations affecting protein structure in children of atomic bomb survivors: preliminary report

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=391733

Enzyme-deficiency variants: frequency and potential significance in human populations

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=391733

Gene mutations (de novo) found in electrophoretic studies of blood protein of infants with anomalous development

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=391733

Erythrocyte enzyme deficiencies assessed with a miniature centrifugal analyzer

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=391733

Elevated frequency of carriers for triosephosphate isomerase deficiency in newborn infants

20 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/6591202

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.81.17.5499

1 reference

21 August 2017

0 references

1 reference

21 August 2017

1 reference

PMCID

391733