bibliographicCitation |
Pillar N, Pleniceanu O, Fang M, Ziv L, Lahav E, Botchan S, Cheng L, Dekel B, Shomron N. A rare variant in the FHL1 gene associated with X-linked recessive hypoparathyroidism. Human Genetics. 2017 Apr 25;136(7):835–45. doi: 10.1007/s00439-017-1804-9. |