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首頁(yè)   >>   技術(shù)文章   >>   Coriell人類(lèi)基因組DNA標(biāo)準(zhǔn)品(GM05114)現(xiàn)貨供應(yīng)

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Coriell人類(lèi)基因組DNA標(biāo)準(zhǔn)品(GM05114)現(xiàn)貨供應(yīng)

閱讀:712      發(fā)布時(shí)間:2024-4-25
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產(chǎn)品名稱(chēng):Coriell人類(lèi)基因組DNA標(biāo)準(zhǔn)品(GM05114)現(xiàn)貨供應(yīng)

產(chǎn)品貨號(hào):GM05114

產(chǎn)品品牌:Coriell

Description:

MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD
DYSTROPHIN; DMD

Affected:Yes

Sex:Male

Age:22 YR (At Sampling)

Overview

l RepositoryNIGMS Human Genetic Cell Repository

l SubcollectionHeritable Diseases  Muscular Dystrophies

l ClassCongenital Muscle Diseases

l Biopsy SourceUnspecified

l Cell Type Fibroblast

l Tissue TypeSkin

l TransformantUntransformed

l Sample SourceFibroblast from Skin, Unspecified

l RaceWhite

l Family Member2

l Relation to Probandbrother

l ConfirmationClinical summary/Case history

l SpeciesHomo sapiens

l Common NameHuman

l RemarksClinically affected with Duchenne muscular dystrophy; diagnosed at age 10; calf hypertrophy; progressive muscle weakness; toe walking, difficulty with stairs and frequent falls noted at age 4; wheelchair bound by age 10; by age 15 there was mild scoliosis, lumbar lordosis, contractures of the elbows, ankles, hips and knees, marked weakness in upper extremities, tight heelcords; by age 20 there was inability to flex hips against gravity, inability to raise hands above head; donor subject has a deletion of exon 45 in the dystrophin gene as determined by multiplex PCR; affected brother is GM05112/13; son of GM05116/17 (mother) and GM05118/19 (father); elevated CPK; same donor as GM05115 (lymphocyte).

歡迎訂購(gòu):

貨號(hào)

產(chǎn)品名稱(chēng)

GM05114

GM05114Fibroblast from Skin, Unspecified

天津益元利康生物科技有限公司現(xiàn)貨供應(yīng)Coriell人類(lèi)基因組DNA標(biāo)準(zhǔn)品(GM05114),歡迎選購(gòu)!

Coriell人類(lèi)基因組DNA標(biāo)準(zhǔn)品(GM05114)現(xiàn)貨供應(yīng)


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