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

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Bibliographic Details
Title:	A rare variant in the FHL1 gene associated with X-linked recessive hypoparathyroidism.
Authors:	Pillar N; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel., Pleniceanu O; 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., Fang M; BGI-Yunnan, Kunming, China., Ziv L; Sheba Cancer Research Center, Sheba Medical Center, Tel Hashomer, Israel., Lahav E; Pediatric Stem Cell Research Institute & Division of Pediatric Nephrology, Edmond & Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel., Botchan S; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel., Cheng L; BGI-Yunnan, Kunming, China. chengle@genomics.cn., Dekel B; 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., Shomron N; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. nshomron@post.tau.ac.il.
Source:	Human genetics [Hum Genet] 2017 Jul; Vol. 136 (7), pp. 835-845. Date of Electronic Publication: 2017 Apr 25.
Publication Type:	Journal Article; Research Support, Non-U.S. Gov't
Journal Info:	Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-1203 (Electronic) Linking ISSN: 03406717 NLM ISO Abbreviation: Hum Genet Subsets: MEDLINE
Database:	MEDLINE Ultimate

Description
ISSN:	1432-1203
DOI:	10.1007/s00439-017-1804-9