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pro vyhledávání: '"粘芳馨"'
Autor:
Fang-Shin Nian, 粘芳馨
107
Mutations in the proline-rich transmembrane protein 2 (PRRT2) gene cause a wide spectrum of neurological diseases, including Paroxysmal Kinesigenic Dyskinesia (PKD) to mental retardation and epilepsy which implicated that PRRT2 might play an
Mutations in the proline-rich transmembrane protein 2 (PRRT2) gene cause a wide spectrum of neurological diseases, including Paroxysmal Kinesigenic Dyskinesia (PKD) to mental retardation and epilepsy which implicated that PRRT2 might play an
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/37e2mx
Autor:
Fang-Shin Nian, 粘芳馨
102
Mutations in RAB18, a member of small G-protein, cause Warburg Micro syndrome, whose clinical features include vision impairment, postnatal microcephaly and lower-limb spasticity. Despite the severity of this devastating disorder, its etiolo
Mutations in RAB18, a member of small G-protein, cause Warburg Micro syndrome, whose clinical features include vision impairment, postnatal microcephaly and lower-limb spasticity. Despite the severity of this devastating disorder, its etiolo
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/68081735099336214983