| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8681849 | Clinical Neurology and Neurosurgery | 2018 | 13 Pages |
Abstract
Patients with NLSDM display clinical heterogeneities despite sharing the same mutation (c.757â¯+â¯1Gâ¯>â¯T) of the PNPLA2 gene, may suggest a founder effect in the region.
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Authors
Jiaze Tan, Haitao Yang, Jingchuan Fan, Yulan Fan, Fei Xiao,