Headache in a middle-aged man due to a rare mutation in the NOTCH 3 gene

Gurung Anil; Bhattacharjee Shakya; Nor Azlisham M.

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Headache in a middle-aged man due to a rare mutation in the NOTCH 3 gene

机译：由于陷波3基因的罕见突变，在中年人中的头痛

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来源
《Neurology India.》 |2019年第3期|共4页
作者
Gurung Anil; Bhattacharjee Shakya; Nor Azlisham M.;
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作者单位

Plymouth Hosp NHS Trust Dept Neurol Plymouth Devon England;

Plymouth Hosp NHS Trust Dept Neurol Plymouth Devon England;

Plymouth Hosp NHS Trust Dept Neurol Plymouth Devon England;

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原文格式 PDF
正文语种 eng
中图分类神经病学与精神病学;
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专利

1. Headache in a middle-aged man due to a rare mutation in the NOTCH 3 gene [J] . Gurung Anil, Bhattacharjee Shakya, Nor Azlisham M. Neurology India. . 2019,第3期

机译：由于陷波3基因的罕见突变，在中年人中的头痛
2. A Japanese Case of CADASIL with a Rare Mutation in Exon 24 of the NOTCH3 Gene [J] . Yuka Ebihara, Hitoshi Mochizuki, Nobuyuki Ishii, Internal medicine. . 2018,第20期

机译：日本案例的Cadasil，在Notch3基因的外显子24中具有罕见突变
3. Considerations on a mutation in the NOTCH3 gene sparing a cysteine residue: A rare polymorphism rather than a CADASIL variant [J] . BersanoA., RanieriM., CiammolaA., Functional neurology . 2012,第4期

机译：保留半胱氨酸残基的NOTCH3基因突变的考虑因素：一种罕见的多态性而不是CADASIL变体
4. Detection of Ultra-Rare Cancer Gene Mutation Using Circulating Cell- Free Tumour DNA in Blood [C] . Guoliang Fu, Sara Temelso, George Sakellariou, International Molecular Medicine Tri-Conference. . 2016

机译：使用血液中循环细胞肿瘤DNA检测超稀有癌基因突变
5. The Notch negative regulatory region: Mutations and mechanisms [D] . Malecki, Michael John 2007

机译：Notch负调控区域：突变和机制
6. A Japanese Case of CADASIL with a Rare Mutation in Exon 24 of the NOTCH3 Gene [O] . Yuka Ebihara, Hitoshi Mochizuki, Nobuyuki Ishii, 2018

机译：日本病例中NOTCH3基因第24外显子罕见突变的CADASIL病例
7. A clinical case of multiple primary cancers in a carrier of rare SDK2 and NOTCH2 gene mutations [O] . Nataliya N. Timoshkina, Dmitry Y. Gvaldin, Ekaterina P. Omelchuk, 2021

机译：罕见的SDK2和Notch2基因突变载体中多次癌症的临床情况

Headache in a middle-aged man due to a rare mutation in the NOTCH 3 gene

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