Identification of a second genetic alteration in patients withSHOXdeficiency individuals: a potential explanation for phenotype variability

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journal：European Journal of Endocrinology

Authors：Naiara C B Dantas; Mariana F A Funari; Antonio M Lerário; Nathalia L M Andrade; Raíssa C Rezende; Laurana P Cellin; Crésio Alves; Lindiane G Crisostomo; Ivo J P Arnhold; Berenice Mendonca; Renata C Scalco; Alexander A L Jorge

Published date：2023-9-1

DOI：10.1093/ejendo/lvad128

PDF link：https://academic.oup.com/ejendo/ ... 1516055/lvad128.pdf

Article link：https://doi.org/10.1093/ejendo/lvad128

Article Source：Oxford University Press (OUP)。

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[Oxford] Identification of a second genetic alteration in patients withSHOXdeficiency individuals: a potential explanation for phenotype variability