Congenital sucrase-isomaltase deficiency: identification of a common Inuit founder mutation. - Wikidata - awgldk - TriplyDB

Congenital sucrase-isomaltase deficiency: identification of a common Inuit founder mutation.

Congenital sucrase-isomaltase deficiency: identification of a common Inuit founder mutation.

http://www.wikidata.org/entity/Q35032399

about

Diagnosing and Treating Intolerance to Carbohydrates in Children Old meets new: identifying founder mutations in genetic disease.The Effect of an Extreme and Prolonged Population Bottleneck on Patterns of Deleterious Variation: Insights from the Greenlandic Inuit.

P2860

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P2860

Congenital sucrase-isomaltase deficiency: identification of a common Inuit founder mutation.

http://www.wikidata.org/entity/Q35032399

description

2014 nî lūn-bûn

@nan

2014 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

Congenital sucrase-isomaltase ...... common Inuit founder mutation.

@ast

Congenital sucrase-isomaltase ...... common Inuit founder mutation.

@en

type

label

Congenital sucrase-isomaltase ...... common Inuit founder mutation.

@ast

Congenital sucrase-isomaltase ...... common Inuit founder mutation.

@en

prefLabel

Congenital sucrase-isomaltase ...... common Inuit founder mutation.

@ast

Congenital sucrase-isomaltase ...... common Inuit founder mutation.

@en

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Canadian Medical Association Journal

P1476

Congenital sucrase-isomaltase ...... common Inuit founder mutation.

@en

P2093

Adam D McIntyre

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C Ronald Scott

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Julien L Marcadier

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Kheirie Issa

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Margaret Boland

http://www.w3.org/2001/XMLSchema#string

Matthew A Lines

http://www.w3.org/2001/XMLSchema#string

Michael T Geraghty

http://www.w3.org/2001/XMLSchema#string

Zaining Wu

http://www.w3.org/2001/XMLSchema#string

P2860

Novel mutations in the human sucrase-isomaltase gene (SI) that cause congenital carbohydrate malabsorption

Sacrosidase therapy for congenital sucrase-isomaltase deficiency

Clinical Aspects and Treatment of Congenital Sucrase-Isomaltase Deficiency

Four Mutations in the SI Gene Are Responsible for the Majority of Clinical Symptoms of CSID

The Human Gene Mutation Database: building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine

Eating habits of a population undergoing a rapid dietary transition: portion sizes of traditional and non-traditional foods and beverages consumed by Inuit adults in Nunavut, Canada.

Dietary habits of Aboriginal children.

Congenital sucrase-isomaltase deficiency.

Sucrase deficiency in Greenland. Incidence and genetic aspects.

Disaccharidase activities in dyspeptic children: biochemical and molecular investigations of maltase-glucoamylase activity.

P304

102-107

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scholarly article

P356

10.1503/CMAJ.140657

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P407

P433

2

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P478

187

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Robert A. Hegele

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2014-12-01T00:00:00Z

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269179768

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