One Novel 2.43Kb Deletion and One Single Nucleotide Mutation of the INSR Gene in a Chinese Neonate with Rabson-Mendenhall Syndrome
中国一名患有Rabson-Mendenhall综合征的新生儿INSR基因中发现一个2.43Kb的新缺失和一个单核苷酸突变
期刊:J Clin Res Pediatr Endocrinol
影响因子:1.500
doi:10.4274/jcrpe.5080.
Xiang Chen ,Huijun Wang ,Bingbing Wu ,Xinran Dong ,Bo Liu ,Hongbo Chen ,Yulan Lu ,Wenhao Zhou ,Lin Yang
