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Article

NPR2 gene variants in familial short stature: a single-center study.

Journal of pediatric endocrinology & metabolism : JPEM - 23 Feb 2022

Yuan Ke, Chen Jiao, Chen Qingqing, Chen Hong, Zhu Jianfang, Fang Yanlan, Wang Chunlin

Abstract excerpt

OBJECTIVES: NPR2 variants are associated with various short stature and bone dysplasia, such as acromesomelic dysplasia Maroteaux tyoe, individuals with a phenotype similar to Léri-Weill syndrome (LWD), and idiopathic short stature (ISS). However, few studies have reported on the relationship between familial short stature (FSS) and NPR2 variants. This study aimed to explore the relationship between FSS and NPR2...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 34565054
DOI: 10.1515/jpem-2021-0332

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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