R54C mutation of NOTCH3 gene in the first Rungus family with CADASIL

R54C mutation of NOTCH3 gene in the first Rungus family with CADASIL

Cerebral autosomal dominant arteriopathy with subcortical infarcts andleukoencephalopathy (CADASIL) is a rare hereditary stroke caused by mutations in NOTCH3 gene.We report the first case of CADASIL in an indigenous Rungus(Kadazan-Dusun) family in Kudat, Sabah, Malaysia confirmed by a R54C (c.160C&g...

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Bibliografiska uppgifter
Huvudupphovsmän: Lim, Kheng Seang, Ai-HueyTan, Lim, Chun Shen, Chua, Kek Heng, Lee, Ping Chin, Norlisah Ramli, Giri Shan Rajahram, Fatimah Tina Hussin, Kum, Thong Wong, Meenakshi Bhattacharjee, Ng, Ching Ching
Materialtyp: Artikel
Språk:English
English
Publicerad: Public Library Science 2015
Ämnen:
QH Natural history
Länkar:https://eprints.ums.edu.my/id/eprint/21418/1/R54C%20mutation%20of%20NOTCH3%20gene%20in%20the%20first%20Rungus%20family%20with%20CADASIL.pdf
https://eprints.ums.edu.my/id/eprint/21418/7/R54C%20mutation%20of%20NOTCH3%20gene%20in%20the%20first%20Rungus%20family%20with%20CADASIL.pdf

Internet

https://eprints.ums.edu.my/id/eprint/21418/1/R54C%20mutation%20of%20NOTCH3%20gene%20in%20the%20first%20Rungus%20family%20with%20CADASIL.pdf
https://eprints.ums.edu.my/id/eprint/21418/7/R54C%20mutation%20of%20NOTCH3%20gene%20in%20the%20first%20Rungus%20family%20with%20CADASIL.pdf

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