| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8310127 | Clinica Chimica Acta | 2016 | 6 Pages |
Abstract
We detected a novel mutation in CLDN16 for the first time. The clinical and genetic findings from this study will help to expand the understanding of this rare disease, FHHNC.
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Authors
Fang Lv, Xiao-jie Xu, Jian-yi Wang, Yi Liu, Yan Jiang, Ou Wang, Wei-bo Xia, Xiao-ping Xing, Mei Li,