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A rare variant in the FHL1 gene associated with X-linked recessive hypoparathyroidism.

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第一作者： Nir,Pillar

第一单位： Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

作者： Nir,Pillar ^[1] ; Oren,Pleniceanu ^[2] ; Mingyan,Fang ^[3] ; Limor,Ziv ^[4] ; Einat,Lahav ^[5] ; Shay,Botchan ^[1] ; Le,Cheng ^[6] ; Benjamin,Dekel ^[7] ; Noam,Shomron ^[8]

作者单位： Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. ^[1] Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.;Pediatric Stem Cell Research Institute & Division of Pediatric Nephrology, Edmond & Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel. ^[2] BGI-Yunnan, Kunming, China. ^[3] Sheba Cancer Research Center, Sheba Medical Center, Tel Hashomer, Israel. ^[4] Pediatric Stem Cell Research Institute & Division of Pediatric Nephrology, Edmond & Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel. ^[5] BGI-Yunnan, Kunming, China. chengle@genomics.cn. ^[6] Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Binyamin.Dekel@sheba.health.gov.il.;Pediatric Stem Cell Research Institute & Division of Pediatric Nephrology, Edmond & Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel. Binyamin.Dekel@sheba.health.gov.il. ^[7] Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. nshomron@post.tau.ac.il. ^[8]