Phenotypic profiling in subjects heterozygous for 1 of 2 rare variants in the hypophosphatasia gene (ALPL)

Authors

Daniel R Tilden, Vanderbilt University
Jonathan H Sheehan, Washington University School of Medicine in St. Louis
John H Newman, Vanderbilt University
Jens Meiler, Vanderbilt University
John A Capra, Vanderbilt University
Andrea Ramirez, Vanderbilt University
Jill Simmons, Monroe Carroll Jr. Children's Hospital at Vanderbilt
Kathryn Dahir, Vanderbilt University

Journal

Journal of the Endocrine Society

Publication Date

6-28-2020

Volume

4

Issue

8

First Page

bvaa084

Document Type

Open Access Publication

DOI

10.1210/jendso/bvaa084

Rights and Permissions

Tilden DR, Sheehan JH, Newman JH, Meiler J, Capra JA, Ramirez A, Simmons J, Dahir K. Phenotypic Profiling in Subjects Heterozygous for 1 of 2 Rare Variants in the Hypophosphatasia Gene (ALPL). J Endocr Soc. 2020 Jun 28;4(8):bvaa084. doi.org/10.1210/jendso/bvaa084 This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

Recommended Citation

Tilden, Daniel R; Sheehan, Jonathan H; Newman, John H; Meiler, Jens; Capra, John A; Ramirez, Andrea; Simmons, Jill; and Dahir, Kathryn, "Phenotypic profiling in subjects heterozygous for 1 of 2 rare variants in the hypophosphatasia gene (ALPL)." Journal of the Endocrine Society. 4, 8. bvaa084 (2020).
https://digitalcommons.wustl.edu/open_access_pubs/11961