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ENPP1 gene

Discuss publications and research concerning the ENPP1 gene.

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Related literature

A novel murine model of early calcium pyrophosphate deposition disease based on the TNFRSF11B mutation mimics features of the human disease.
ENPP1
Novel ENPP1 Gene Mutation Causing Generalized Arterial Calcification of Infancy: A case report.
ENPP1
Genome-wide association study in chondrocalcinosis reveals ENPP1 as a candidate therapeutic target in calcium pyrophosphate deposition disease.
ENPP1
The impact of monoallelic inactivation mutations in the ENPP1 gene on pediatric skeletal development: a case report and literature review.
ENPP1
Quantitative correlation of ENPP1 pathogenic variants with disease phenotype.
ENPP1
Condylar geometry variation is associated with ENPP1 variant in a population of patients with dento-facial deformities.
ENPP1
ENPP1 and ESR1 genotypes influence temporomandibular disorders development and surgical treatment response in dentofacial deformities.
ENPP1
Phosphate homeostasis and genetic mutations of familial hypophosphatemic rickets.
ENPP1
Hearing loss is part of the clinical picture of ENPP1 loss of function mutation.
ENPP1
Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases.
ENPP1

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