(Q35199076)

7 August 2017

title

The Hartnup phenotype: Mendelian transport disorder, multifactorial disease (English)

1 reference

7 August 2017

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C R Scriver

1

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7 August 2017

B Mahon

2

1 reference

7 August 2017

H L Levy

3

1 reference

7 August 2017

C L Clow

4

1 reference

7 August 2017

T M Reade

5

1 reference

7 August 2017

J Kronick

6

1 reference

7 August 2017

B Lemieux

7

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7 August 2017

C Laberge

8

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7 August 2017

language of work or name

English

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publication date

1 May 1987

1 reference

American Journal of Human Genetics

7 August 2017

published in

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7 August 2017

volume

40

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7 August 2017

issue

5

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7 August 2017

page(s)

401-412

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A study of the behaviour of some sixty amino-acids and other ninhydrin-reacting substances on phenol-;collidine' filter-paper chromatograms, with notes as to the occurrence of some of them in biological fluids

7 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684147

Hereditary pellagra-like skin rash with temporary cerebellar ataxia, constant renal amino-aciduria, and other bizarre biochemical features

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684147

The molecular basis of dominance.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684147

Effects of amino acid loads on a health infant with the biochemical features of Hartnup disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684147

Absorption of Amino Acids and Peptides in a Child with a Variant of Hartnup Disease and Coexistent Coeliac Disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684147

Transport of dibasic amino acids, cystine, and tryptophan by cultured human fibroblasts: absence of a defect in cystinuria and Hartnup disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684147

Normal plasma free amino acid values in adults: the influence of some common physiological variables.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684147

Natural history of Hartnup disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684147

CLINICAL AND BIOCHEMICAL FEATURES OF A CASE OF HARTNUP DISEASE.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684147

26 September 2018

Genetic heterogeneity

1 reference

12 December 2020

Stature and Nutrition in Cystinuria and Hartnup Disease

1 reference

12 December 2020

Genetics and Medicine: An Evolving Relationship

1 reference

12 December 2020

Hartnup disorder in a New England family

1 reference

12 December 2020

Age at onset and causes of disease

1 reference

12 December 2020

Quantitative Differences and Gene Dosage in the Human Red Cell Acid Phosphatase Polymorphism

1 reference

12 December 2020

Studies of intestinal transport defect in Hartnup disease

1 reference

12 December 2020

Identifiers

PMC publication ID

1684147

1 reference

7 August 2017

1 reference