Rare coding variants in ALPL are associated with low serum alkaline phosphatase and low bone mineral density. - Wikidata - awgldk - TriplyDB

Rare coding variants in ALPL are associated with low serum alkaline phosphatase and low bone mineral density.

Rare coding variants in ALPL are associated with low serum alkaline phosphatase and low bone mineral density.

http://www.wikidata.org/entity/Q37260845

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Osteoporosis in men: findings from the Osteoporotic Fractures in Men Study (MrOS)Systems genetics of metabolism: the use of the BXD murine reference panel for multiscalar integration of traits Molecular diagnosis of hypophosphatasia and differential diagnosis by targeted Next Generation Sequencing.Hypophosphatasia: an overview of the disease and its treatment.Atypical femur fractures: a distinctive tract of adult hypophosphatasia.Genetic analysis of adults heterozygous for ALPL mutations.Mutational and biochemical findings in adults with persistent hypophosphatasemia.

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Rare coding variants in ALPL are associated with low serum alkaline phosphatase and low bone mineral density.

http://www.wikidata.org/entity/Q37260845

description

article científic

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article scientifique

@fr

articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on January 2012

@en

vedecký článok

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vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Rare coding variants in ALPL a ...... and low bone mineral density.

@en

Rare coding variants in ALPL a ...... and low bone mineral density.

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type

label

Rare coding variants in ALPL a ...... and low bone mineral density.

@en

Rare coding variants in ALPL a ...... and low bone mineral density.

@nl

prefLabel

Rare coding variants in ALPL a ...... and low bone mineral density.

@en

Rare coding variants in ALPL a ...... and low bone mineral density.

@nl

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Journal of Bone and Mineral Research

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Rare coding variants in ALPL a ...... e and low bone mineral density

@en

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Amy S Carlos

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

Emily A Larson

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

Joseph M Zmuda

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Robert F Klein

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Wendy J Wagoner

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P2860

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies

Rare independent mutations in renal salt handling genes contribute to blood pressure variation

Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes

Multiple sequence alignment with hierarchical clustering

Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia

An integrative genetics approach to identify candidate genes regulating BMD: combining linkage, gene expression, and association.

Mouse phenome database

Mild forms of hypophosphatasia mostly result from dominant negative effect of severe alleles or from compound heterozygosity for severe and moderate alleles.

Interpretation of association signals and identification of causal variants from genome-wide association studies

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93-103

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scholarly article

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10.1002/JBMR.527

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1

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27

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Carrie M Nielson

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2012-01-01T00:00:00Z

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51678851

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21956185

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3810303

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