Associated Papers
New insights in the genetic variant spectrum of SLC34A2 in pulmonary alveolar microlithiasis; a systematic review.
Jönsson ÅLM et al.
Orphanet Journal of Rare Diseases, 2023
Impaired phosphate transport in SLC34A2 variants in patients with pulmonary alveolar microlithiasis.
Jönsson ÅLM et al.
Human Genomics, 2022
Pulmonary alveolar microlithiasis: no longer in the stone age.
Bendstrup E et al.
Erj Open Research, 2020
Eight novel variants in the SLC34A2 gene in pulmonary alveolar microlithiasis.
Jönsson ÅLM et al.
The European Respiratory Journal, 2020
SLC34A2 Gene mutation of pulmonary alveolar microlithiasis: report of four cases and review of literatures.
Yin X et al.
Respiratory Medicine, 2013
Mutations in SLC34A2 cause pulmonary alveolar microlithiasis and are possibly associated with testicular microlithiasis.
Corut A et al.
American Journal of Human Genetics, 2006
Differences in genetic characteristics between Chinese and non-Chinese patients with pulmonary alveolar microlithiasis-case series and a systematic review.
Guo M et al.
Therapeutic Advances in Respiratory Disease, 0
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