A Chinese family with Noonan syndrome caused by a heterozygous variant in LZTR1: a case report and literature review

被引：0
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作者：
Xiu Zhao
Zhuoguang Li
Li Wang
Zhangzhang Lan
Feifei Lin
Wenyong Zhang
Zhe Su
机构：
[1] Shenzhen Children’s Hospital,Endocrinology Department
[2] School of Medicine,Radiology Department
[3] Southern University of Science and Technology,undefined
[4] Shenzhen Children’s Hospital,undefined
来源：
BMC Endocrine Disorders | / 21卷
关键词：
Noonan syndrome; Autosomal dominant; Growth hormone deficiency;
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