Identification of a novel FUT1 allele with two mutations in a Chinese para-Bombay individual.

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Identification of a novel FUT1 allele with two mutations in a Chinese para-Bombay individual.

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http://www.wikidata.org/entity/Q50220411

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2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年学术文章

@wuu

2016年学术文章

@zh

2016年学术文章

@zh-cn

2016年学术文章

@zh-hans

2016年学术文章

@zh-my

2016年学术文章

@zh-sg

2016年學術文章

@yue

2016年學術文章

@zh-hant

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Identification of a novel FUT1 ...... hinese para-Bombay individual.

@en

Identification of a novel FUT1 ...... hinese para-Bombay individual.

@nl

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Item

label

Identification of a novel FUT1 ...... hinese para-Bombay individual.

@en

Identification of a novel FUT1 ...... hinese para-Bombay individual.

@nl

prefLabel

Identification of a novel FUT1 ...... hinese para-Bombay individual.

@en

Identification of a novel FUT1 ...... hinese para-Bombay individual.

@nl

P1476

Identification of a novel FUT1 ...... hinese para-Bombay individual.

@en

P2093

Chunyan Huang

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Jinzhe Tan

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Li Qin

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Li Tian

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Lixin Wang

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Zengzhen Wei

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P2860

Sequence and expression of a candidate for the human Secretor blood group alpha(1,2)fucosyltransferase gene (FUT2). Homozygosity for an enzyme-inactivating nonsense mutation commonly correlates with the non-secretor phenotype

Polymorphism of the h allele and the population frequency of sporadic nonfunctional alleles

The summary of FUT1 and FUT2 genotyping analysis in Chinese para-Bombay individuals including additional nine probands from Guangzhou in China.

Molecular genetics of H, Se, Lewis and other fucosyltransferase genes.

Prevalence of Bombay blood group in a tertiary care hospital, Andhra Pradesh, India.

Correlation of a missense mutation in the human Secretor alpha 1,2-fucosyltransferase gene with the Lewis(a+b+) phenotype: a potential molecular basis for the weak Secretor allele (Sew).

A novel FUT1 allele was identified in a Chinese individual with para-Bombay phenotype.

Systematic sequence analysis of the human fucosyltransferase 2 (FUT2) gene identifies novel sequence variations and alleles

P304

93-96

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P31

scholarly article

P356

10.1111/TRF.13879

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P433

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P478

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P577

2016-12-27T00:00:00Z

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P698

28026021

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