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New insights in the genetic variant spectrum of SLC34A2 in pulmonary alveolar microlithiasis; a systematic review.
Jönsson ÅLM, Hilberg O, Simonsen U, Christensen JH, Bendstrup E. Jönsson ÅLM, et al. Orphanet J Rare Dis. 2023 May 31;18(1):130. doi: 10.1186/s13023-023-02712-7. Orphanet J Rare Dis. 2023. PMID: 37259144 Free PMC article. Review.
Pulmonary alveolar microlithiasis (PAM) is a rare autosomal recessive lung disease caused by variants in the SLC34A2 gene encoding the sodium-dependent phosphate transport protein 2B, NaPi-2b. ...
Pulmonary alveolar microlithiasis (PAM) is a rare autosomal recessive lung disease caused by variants in the SLC34A2 ge
Pulmonary alveolar microlithiasis: an interesting case report with systematic review of Indian literature.
Ganesan N, Ambroise MM, Ramdas A, Kisku KH, Singh K, Varghese RG. Ganesan N, et al. Front Med. 2015 Jun;9(2):229-38. doi: 10.1007/s11684-015-0394-y. Epub 2015 May 30. Front Med. 2015. PMID: 26024716 Review.
Pulmonary alveolar microlithiasis is a rare disease characterized by intra-alveolar presence of microliths. This study reports an interesting case of pulmonary alveolar microlithiasis and provides a systematic review of cases reported fro
Pulmonary alveolar microlithiasis is a rare disease characterized by intra-alveolar presence of microliths. This study