Linkage of Familial Moyamoya Disease (Spontaneous Occlusion of the Circle of Willis) to Chromosome 17q25 | Zendy

T. Yamauchi | Zendy; Mitsuhiro Tada | Zendy; Kiyohiro Houkin | Zendy; Toshihiro Tanaka | Zendy; Yusuke Nakamura | Zendy; Satoshi Kuroda | Zendy; Hiroshi Abe | Zendy; Takuya Inoue | Zendy; Kiyonobu Ikezaki | Zendy; Toshio Matsushima | Zendy; Masashi Fukui | Zendy

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Linkage of Familial Moyamoya Disease (Spontaneous Occlusion of the Circle of Willis) to Chromosome 17q25

Author(s) -

T. Yamauchi,

Mitsuhiro Tada,

Kiyohiro Houkin,

Toshihiro Tanaka,

Yusuke Nakamura,

Satoshi Kuroda,

Hiroshi Abe,

Takuya Inoue,

Kiyonobu Ikezaki,

Toshio Matsushima,

Masashi Fukui

Publication year - 2000

Publication title -

stroke

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 3.397

H-Index - 319

eISSN - 1524-4628

pISSN - 0039-2499

DOI - 10.1161/01.str.31.4.930

Subject(s) - moyamoya disease , locus (genetics) , microsatellite , genetics , genetic linkage , medicine , polymerase chain reaction , chromosome , genetic marker , neurofibromatosis , chromosome 21 , chromosome 17 (human) , gene , allele , biology

Moyamoya disease is a cerebrovascular disease of unknown cause that mainly affects Japanese children. The incidence of familial occurrence accounts for 9% of cases. The characteristic lesions of moyamoya disease are occasionally seen in neurofibromatosis type 1, of which the causative gene (NF1) has been assigned to chromosome 17q11.2.

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