產(chǎn)品(pǐn)名稱
：Coriell人類基因組DNA標(biāo)準(zhǔn)品(GM05017)現(xiàn)貨供應

產品貨號
：GM05017

產品品牌(pái)
：Coriell

Description:

MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD
DYSTROPHIN; DMD

Affected:Yes

Sex:Male

Age:12 YR (At Sampling)

Overview
：

Repository
：NIGMS Human Genetic Cell Repository

Subcollection
：Heritable Diseases  Muscular Dystrophies  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; diagnosis made at age 4; progressive muscular dystrophy; weakness; waddling gait noted at age 4 and subsequent progressive deterioration in walking ability; wheelchair bound by age 10; at age 10 there was good upper arm strength, no scoliosis, inability to lift leg off wheelchair pad; son of GM05022/23; elevated CPK; muscle biopsy performed but results unavailable; donor subject has a deletion of exons 45-50 in the dystrophin gene as determined by multiplex PCR; same donor as GM05016 (lymphocyte).

歡迎訂購(gòu)
：

天(tiān)津(jīn)益元利(lì)康生物科技(jì)有限(xiàn)公(gōng)司(sī)現貨(huò)供(gōng)應Coriell人(rén)類基因組(zǔ)DNA標(biāo)準品(pǐn)(GM05017)，歡迎(yíng)選購！