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      當(dāng)前位置:首頁(yè)技術(shù)文章Coriell人類基因組DNA標(biāo)準(zhǔn)品(GM05114)現(xiàn)貨供應(yīng)

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

      更新時(shí)間:2024-04-25點(diǎn)擊次數(shù):1189

      產(chǎn)品名稱:Coriell人類基因組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

      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人類基因組DNA標(biāo)準(zhǔn)品(GM05114),歡迎選購(gòu)!

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


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