共 50 条
- [31] Novel intronic mutation of MEN1 gene causing familial isolated primary hyperparathyroidism JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (08): : 4124 - 4129
- [33] A novel SLC20A2 gene mutation causing primary familial brain calcification in an Ukrainian patient Neurological Sciences, 2019, 40 : 1283 - 1285
- [35] Neuropsychological heterogeneity in patients with primary familial brain calcification due to a novel mutation in SLC20A2 Neurological Sciences, 2018, 39 : 379 - 380
- [36] Primary familial brain calcification in a Norwegian family, caused by a novel SLC20A2 gene mutation Journal of Neurology, 2016, 263 : 594 - 596
- [40] Vertical Supranuclear Gaze Palsy in Primary Familial Brain Calcification Associated with a Novel SLC20A2 Mutation MOVEMENT DISORDERS CLINICAL PRACTICE, 2023, 10 (03): : 501 - 503