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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(GM04364)現(xiàn)貨供應(yīng)

        Coriell人類(lèi)基因組DNA標(biāo)準(zhǔn)品(GM04364)現(xiàn)貨供應(yīng)

         更新時(shí)間:2024-04-25    點(diǎn)擊量:674

        產(chǎn)品名稱(chēng):Coriell人類(lèi)基因組DNA標(biāo)準(zhǔn)品(GM04364)現(xiàn)貨供應(yīng)

        產(chǎn)品貨號(hào):GM04364

        產(chǎn)品品牌:Coriell

        Description:

        MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD
        DYSTROPHIN; DMD

        Affected:Yes

        Sex:Male

        Age:13 YR (At Sampling)

        Overview

        Repository:NIGMS Human Genetic Cell Repository

        Subcollection:Heritable Diseases  Muscular Dystrophies  GeT-RM Samples dbGaP

        Class:Congenital Muscle Diseases

        Biopsy Source:Unspecified

        Cell Type:Fibroblast

        Tissue Type:Skin

        Transformant:Untransformed

        Sample Source:Fibroblast from Skin, Unspecified

        Race:White

        Family Member:1

        Relation to Proband:proband

        Confirmation:Clinical summary/Case history

        Species:Homo sapiens

        Common Name:Human

        Remarks:Clinically affected with Duchenne muscular dystrophy; diagnosed sometime before age 10; calf hypertrophy; Gower's maneuver; ambulatory at age 10; muscle testing at age 10 showed most muscles to be in fair to poor range but good muscle power demonstrated in hamstrings, posterior and anterior tibs and upper trapezius; at age 10 there were tight heelcords, tightness of the hip flexors, hamstrings and knees; son of GM04363; elevated CPK; muscle biopsy showed classical histological findings of Duchenne muscular dystrophy; donor subject shows a deletion of exons 51-55 of the dystrophin gene by multiplex ligation probe amplification (MLPA) analysis.


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        貨號(hào)

        產(chǎn)品名稱(chēng)

        GM04364

        GM04364Fibroblast 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(GM04364),歡迎選購(gòu)!

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