Display Settings:

Format

Send to:

Choose Destination
See comment in PubMed Commons below
Am J Respir Crit Care Med. 2007 Feb 1;175(3):263-8. Epub 2006 Nov 9.

Mutations in the SLC34A2 gene are associated with pulmonary alveolar microlithiasis.

Author information

  • 1Departments of Respiratory Medicine, Pathology, and Chest Surgery, Saitama Medical University, Saitama, Japan.

Abstract

RATIONALE:

Pulmonary alveolar microlithiasis is an autosomal recessive disorder in which microliths are formed in the alveolar space.

OBJECTIVES:

To identify the responsible gene that causes pulmonary alveolar microlithiasis.

METHODS:

By means of a genomewide single-nucleotide polymorphism analysis using DNA from three patients, we have narrowed the region in which the candidate gene is located. From this region, we have identified a gene that has mutations in all patients with pulmonary alveolar microlithiasis.

MEASUREMENTS AND MAIN RESULTS:

We identified a candidate gene, SLC34A2, that encodes a type IIb sodium phosphate cotransporter and that is mutated in six of six patients investigated. SLC34A2 is specifically expressed in type II alveolar cells, and the mutations abolished the normal gene function.

CONCLUSION:

Mutations in the SLC34A2 gene that abolish normal gene function cause pulmonary alveolar microlithiasis.

PMID:
17095743
[PubMed - indexed for MEDLINE]
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for Atypon
    Loading ...
    Write to the Help Desk