2Anglin RE,Garside SL,Tarnopolsky MA, et al. The psychiatricmanifestations of mitochondrial disorders: a case and review ofthe literature[J]. J Clin Psychiatry,2012,73(4) : 506-512. 被引量：1
3Finsterer J, Zarrouk Mahjoub S. Leukoencephalopathies inmitochondrial disorders: clinical and MRI findings [ J]. JNeuroimaging,2012,22(3) :el-11. 被引量：1
1[2]Cobben JM et al,Confirmation of clinical diagnosis in requests for prenatal prediction of SMA type Ⅰ[J].J Neurol Neurosurg Psychiatry,1993,56:319. 被引量：1
2[5]Lefebvre S,Burglen L,Reboulltt S,et al.Identification and characterization of spinal muscular atrophy-determining gene[J].Cell,1995,80:155. 被引量：1
3[6]Roy N,Mahadeevan MS,McLean M,et al.The gene for neuronal apoptosis inhibitory protein is partially deleted in individuals with spinal muscular atrophy[J].Cell,1995,80:167. 被引量：1
4Bhuvaneswar C G, Coetz J L, Stern T A. Multiple neuro- logic, psychiatric, and endocrine complaints in a young woman: a case discussion and review of the clinical fea- tures and management of mitochondrial myopathy, en- cephalopathy, lactic acidosis, and stroke[ J]. Prim Care Companion J Clin Psychiatry, 2008,10 ( 3 ) :2374244. 被引量：1
5Hirano M, Ricci E, Koenigsberger M R, et al. MELAS: an original and clinical critelia for diagnosisi [ J ]. Neuro- muse Disord, 1992,2(2) :125-135. 被引量：1
6Kanaumi T, Hirose S, Goto Y, et al. An infant with a mitochondrial A3243G mutation demonstrating the MELAS phenoty[J]. Pediatr Neurol, 2006,34 ( 3 ) : 235- 238. 被引量：1
7Thambisetty M, Newman N J. Diagnosis and management of MELAS[J]. Expert Rev Mol Diagn, 2004,4(5):631-644. 被引量：1
