(Q45017396)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15309681%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

title

Identification of a common mutation in mucopolysaccharidosis IVA: correlation among genotype, phenotype, and keratan sulfate (English)

1 reference

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31 December 2019

1 reference

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31 December 2019

Roberto Giugliani

1 reference

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31 December 2019

Shunji Tomatsu

1 reference

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31 December 2019

Tatiana Dieter

1 reference

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31 December 2019

Ida V Schwartz

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31 December 2019

Piedad Sarmient

1 reference

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31 December 2019

Luis A Barrera

1 reference

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31 December 2019

Norberto Guelbert

1 reference

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31 December 2019

Raquel Kremer

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31 December 2019

Monica A Gutierrez

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31 December 2019

Tatsuo Nishioka

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31 December 2019

Olga Peña Serrato

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31 December 2019

Adriana Maria Montaño

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31 December 2019

Seiji Yamaguchi

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31 December 2019

Akihiko Noguchi

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31 December 2019

publication date

11 August 2004

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Journal of Human Genetics

31 December 2019

published in

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31 December 2019

volume

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31 December 2019

issue

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31 December 2019

page(s)

490-494

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Identification of 31 novel mutations in the N-acetylgalactosamine-6-sulfatase gene reveals excessive allelic heterogeneity among patients with Morquio A syndrome

31 December 2019

cites work

1 reference

12 December 2020

Morquio disease: isolation, characterization and expression of full-length cDNA for human N-acetylgalactosamine-6-sulfate sulfatase

1 reference

12 December 2020

Molecular heterogeneity in mucopolysaccharidosis IVA in Australia and Northern Ireland: nine novel mutations including T312S, a common allele that confers a mild phenotype

1 reference

12 December 2020

The multiple sulfatase deficiency gene encodes an essential and limiting factor for the activity of sulfatases

1 reference

12 December 2020

Biochemical and structural analysis of missense mutations in N-acetylgalactosamine-6-sulfate sulfatase causing mucopolysaccharidosis IVA phenotypes

1 reference

12 December 2020

Multiple sulfatase deficiency is caused by mutations in the gene encoding the human C(alpha)-formylglycine generating enzyme

1 reference

12 December 2020

Mucopolysaccharidosis IVA: polymorphic haplotypes and informative RFLPs in the Japanese population

1 reference

12 December 2020

Fifteen polymorphisms in the N-acetylgalactosamine-6-sulfate sulfatase (GALNS) gene: diagnostic implications in Morquio disease

1 reference

12 December 2020

Development and testing of new screening method for keratan sulfate in mucopolysaccharidosis IVA.

1 reference

12 December 2020

Mucopolysaccharidosis IVA: characterization of a common mutation found in Finnish patients with attenuated phenotype

1 reference

12 December 2020

Mucopolysaccharidosis IV A: molecular cloning of the human N-acetylgalactosamine-6-sulfatase gene (GALNS) and analysis of the 5'-flanking region

1 reference

12 December 2020

Fourteen novel mucopolysaccharidosis IVA producing mutations in GALNS gene

1 reference

12 December 2020

Mucopolysaccharidosis IVA: identification of a common missense mutation I113F in the N-Acetylgalactosamine-6-sulfate sulfatase gene

1 reference

12 December 2020

Mucopolysaccharidosis IVA: screening and identification of mutations of the N-acetylgalactosamine-6-sulfate sulfatase gene

1 reference

12 December 2020

Mucopolysaccharidosis type IVA. N-acetylgalactosamine-6-sulfate sulfatase exonic point mutations in classical Morquio and mild cases

1 reference

12 December 2020

10.1007/S10038-004-0178-8

Identifiers

DOI

1 reference

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Dimensions Publication ID

31 December 2019

1005870007

0 references

1 reference

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