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Fig. 4 | Orphanet Journal of Rare Diseases

Fig. 4

From: New insights in the genetic variant spectrum of SLC34A2 in pulmonary alveolar microlithiasis; a systematic review

Fig. 4

Allelic variants in SLC34A2 in PAM patients reported in the literature [2, 3, 5, 6, 35, 43, 73,74,75,76,77,78,79,80,81,82,83,84,85,86,87,88,89,90,91,92,93,94]. Red small squares represent the number of families in which the individual variants are found. Narrow box for non-coding exon and wider box for coding exon. Exons, introns, and deletions are not drawn to scale. Variants are present in homozygous form unless otherwise stated

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