| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8689867 | Neuromuscular Disorders | 2018 | 8 Pages |
Abstract
- A novel missense mutation in the lactate dehydrogenase A gene (LDHA) was identified in a Chinese family with glycogenosis type XI.
- Annular erythematous lesions with desquamating borders are typical.
- Recognition of skin manifesitation can be indicative to the diagnosis.
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Authors
Dongyue Yue, Wenhua Zhu, Chongbo Zhao,