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本文引用的文献

1
A case with a 120 base pair insertional mutation in the prion protein gene: the first case in Japan.一例朊病毒蛋白基因存在120个碱基对插入突变的病例:日本首例。
J Neurol Neurosurg Psychiatry. 2005 May;76(5):756-7. doi: 10.1136/jnnp.2004.048553.
2
Octapeptide repeat insertions in the prion protein gene and early onset dementia.朊蛋白基因中的八肽重复序列插入与早发性痴呆
J Neurol Neurosurg Psychiatry. 2004 Aug;75(8):1166-70. doi: 10.1136/jnnp.2003.020198.
3
Prominent psychiatric features and early onset in an inherited prion disease with a new insertional mutation in the prion protein gene.一种在朊病毒蛋白基因中存在新插入突变的遗传性朊病毒病的显著精神症状和早发情况。
Brain. 1999 Dec;122 ( Pt 12):2375-86. doi: 10.1093/brain/122.12.2375.
4
Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene.与PRNP基因中五个、七个和八个额外八肽编码重复序列相关的可传播性家族性克雅氏病。
Proc Natl Acad Sci U S A. 1991 Dec 1;88(23):10926-30. doi: 10.1073/pnas.88.23.10926.

De novo seven extra repeat expanded mutation in the PRNP gene in an Italian patient with early onset dementia.

作者信息

Cannella M, Martino T, Simonelli M, Ciammola A, Gradini R, Ciarmiello A, Gianfrancesco F, Squitieri F

出版信息

J Neurol Neurosurg Psychiatry. 2007 Dec;78(12):1411-3. doi: 10.1136/jnnp.2007.121137. Epub 2007 Aug 6.

DOI:10.1136/jnnp.2007.121137
PMID:17682007
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2095619/
Abstract
摘要