| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8813572 | Pediatrics & Neonatology | 2016 | 7 Pages |
Abstract
Compared with other countries, the estimated incidence of NKH was relatively rare in the Taiwanese population. It is important to characterize all index cases at the genetic level. With more awareness of NKH, increased knowledge of gene mutation, and improvement of diagnostic tools, NKH can be diagnosed more accurately.
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Authors
Chiao-Fan Chiu, Ju-Li Lin, Jainn-Jim Lin, Min-Hua Tseng, Fu-Sung Lo, Ming-Chou Chiang,