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- [5] A CASE OF CONGENITAL GENERALIZED LIPODYSTROPHY TYPE 2 WITH NOVEL BSCL2 GENE MUTATION HORMONE RESEARCH IN PAEDIATRICS, 2017, 88 : 141 - 142
- [8] Deletion mutation in BSCL2 gene underlies congenital generalized lipodystrophy in a Pakistani family Diagnostic Pathology, 8
- [10] Parkinson's Disease 2 The pathogenesis of Parkinson's disease LANCET, 2024, 403 (10423): : 293 - 304