Literature DB >> 35349104

X-linked osteogenesis imperfecta accompanied by patent ductus arteriosus: a case with a novel splice variant in PLS3.

Chuang Qiu1, Qi-Wei Li2, Lu Zhang3, Xiao-Liang Liu4.   

Abstract

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Year:  2022        PMID： 35349104     DOI： 10.1007/s12519-022-00539-z

Source DB:  PubMed          Journal:  World J Pediatr            Impact factor:   9.186


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  2 in total

1.  Teriparatide Treatment in Patients With WNT1 or PLS3 Mutation-Related Early-Onset Osteoporosis: A Pilot Study.

Authors:  Ville-Valtteri Välimäki; Outi Mäkitie; Renata Pereira; Christine Laine; Katherine Wesseling-Perry; Jorma Määttä; Mikko Kirjavainen; Heli Viljakainen; Matti J Välimäki
Journal:  J Clin Endocrinol Metab       Date:  2017-02-01       Impact factor: 5.958

2.  A novel mutation in PLS3 causes extremely rare X-linked osteogenesis imperfecta.

Authors:  Jing Hu; Lu-Jiao Li; Wen-Bin Zheng; Di-Chen Zhao; Ou Wang; Yan Jiang; Xiao-Ping Xing; Mei Li; Weibo Xia
Journal:  Mol Genet Genomic Med       Date:  2020-11-09       Impact factor: 2.183
  2 in total

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