(Q24679512)

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Sequencing of the variant thyroxine-binding globulin (TBG)-Quebec reveals two nucleotide substitutions

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title

Sequencing of the variant thyroxine-binding globulin (TBG)-Quebec reveals two nucleotide substitutions (English)

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author name string

R Bertenshaw

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1

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K Takeda

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2

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S Refetoff

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3

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language of work or name

English

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publication date

April 1991

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published in

American Journal of Human Genetics

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volume

48

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issue

4

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page(s)

741-4

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cites work

Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS)

1 reference

stated in

PubMed Central

reference URL

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retrieved

7 April 2017

Sequence of the variant thyroxine-binding globulin of Australian aborigines. Only one of two amino acid replacements is responsible for its altered properties

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682945

retrieved

7 April 2017

Polymorphic DNA region adjacent to the 5' end of the human insulin gene

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682945

retrieved

7 April 2017

Localization of the human thyroxine-binding globulin gene to the long arm of the X chromosome (Xq21-22).

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682945

retrieved

28 September 2017

Two new inherited defects of the thyroxine-binding globulin (TBG) molecule presenting as partial TBG deficiency

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682945

retrieved

28 September 2017

Replacement of Leu227 by Pro in thyroxine-binding globulin (TBG) is associated with complete TBG deficiency in three of eight families with this inherited defect

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682945

retrieved

28 September 2017

Molecular basis for the properties of the thyroxine-binding globulin-slow variant in American blacks

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682945

retrieved

28 September 2017

Hereditary abnormalities of thyroxine-binding globulin concentration. A study of 19 kindreds with inherited increase or decrease of thyroxine-binding globulin

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1901689

retrieved

12 December 2020

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OpenCitations bibliographic resource ID

862134

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stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

862134

PubMed publication ID

1901689

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

862134

(Q24679512)

Sequencing of the variant thyroxine-binding globulin (TBG)-Quebec reveals two nucleotide substitutions

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