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A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
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[Clinical and genetic characteristics of Gitelman syndrome in 5 pedigrees]

R R Shi, C C Li, L Fang

  • 1Department of Endocrinology, Shandong Provincial Hospital Affiliated to Shandong University, Shandong Clinical Medical Center of Endocrinology and Metabolism, Institute of Endocrinology and Metabolism, Shandong Academy of Clinical Medicine, Ji'nan 250000, China.

Zhonghua Nei Ke Za Zhi
|February 7, 2017
PubMed

Keywords:
Gitelman syndromeMutationSLC12A3 gene

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