(Q46936233)

English

Clinical and genetic analysis for a Chinese family with hereditary fructose intolerance

scientific article published in August 2007

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1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17955389

Clinical and genetic analysis for a Chinese family with hereditary fructose intolerance (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17955389

author name string

Zhen-Ni Chi

1

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17955389

Jie Hong

2

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17955389

Jun Yang

3

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17955389

Hui-Jie Zhang

4

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17955389

Meng Dai

5

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17955389

Bin Cui

6

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17955389

Yu Zhang

7

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17955389

Wei-Qiong Gu

8

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17955389

Yi-Fei Zhang

9

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17955389

Qiao-Rui Liu

10

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17955389

Wei-Qing Wang

11

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17955389

Xiao-Ying Li

12

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17955389

Guang Ning

13

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17955389

publication date

1 August 2007

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Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17955389

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17955389

32

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Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17955389

1

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17955389

122-126

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Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17955389

An EST and STS-based YAC contig map of human chromosome 9q22.3

1 reference

https://pubmed.ncbi.nlm.nih.gov/17955389

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular evidence for compound heterozygosity in hereditary fructose intolerance

1 reference

https://pubmed.ncbi.nlm.nih.gov/17955389

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The spectrum of aldolase B (ALDOB) mutations and the prevalence of hereditary fructose intolerance in Central Europe.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17955389

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structure of the thermolabile mutant aldolase B, A149P: molecular basis of hereditary fructose intolerance

1 reference

https://pubmed.ncbi.nlm.nih.gov/17955389

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary fructose intolerance.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17955389

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular analysis of common aldolase B alleles for hereditary fructose intolerance in North Americans

1 reference

https://pubmed.ncbi.nlm.nih.gov/17955389

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The molecular basis of hereditary fructose intolerance in Italian children

1 reference

https://pubmed.ncbi.nlm.nih.gov/17955389

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular basis of hereditary fructose intolerance in Italy: identification of two novel mutations in the aldolase B gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/17955389

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel six-nucleotide deletion in the hepatic fructose-1,6-bisphosphate aldolase gene in a patient with hereditary fructose intolerance and enzyme structure-function implications

1 reference

https://pubmed.ncbi.nlm.nih.gov/17955389

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparative use of glucose and fructose in cultured fibroblasts from patients with hereditary fructose intolerance

1 reference

https://pubmed.ncbi.nlm.nih.gov/17955389

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

IDIOSYNCRASY TO FRUCTOSE

1 reference

https://pubmed.ncbi.nlm.nih.gov/17955389

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of the human aldolase B gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/17955389

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular basis of hereditary fructose intolerance: mutations and polymorphisms in the human aldolase B gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/17955389

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary fructose intolerance

1 reference

https://pubmed.ncbi.nlm.nih.gov/17955389

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complete amino acid sequence for human aldolase B derived from cDNA and genomic clones

1 reference

https://pubmed.ncbi.nlm.nih.gov/17955389

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S12020-007-9013-2

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17955389

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17955389

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