產品(pǐn)名(míng)稱(chēng)：Coriell人(rén)類基因(yīn)組DNA標準(zhǔn)品(GM05114)現(xiàn)貨供應(yīng)

產品(pǐn)貨(huò)號(hào)：GM05114

產(chǎn)品品(pǐn)牌：Coriell

Description:

MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD
DYSTROPHIN; DMD

Affected:Yes

Sex:Male

Age:22 YR (At Sampling)

Overview：

l Repository：NIGMS Human Genetic Cell Repository

l Subcollection：Heritable Diseases  Muscular Dystrophies

l Class：Congenital Muscle Diseases

l Biopsy Source：Unspecified

l Cell Type： Fibroblast

l Tissue Type：Skin

l Transformant：Untransformed

l Sample Source：Fibroblast from Skin, Unspecified

l Race：White

l Family Member：2

l Relation to Proband：brother

l Confirmation：Clinical summary/Case history

l Species：Homo sapiens

l Common Name：Human

l Remarks：Clinically 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(yíng)訂(dìng)購(gòu)：

天津(jīn)益(yì)元(yuán)利康生(shēng)物科技(jì)有限公司(sī)現貨供(gōng)應Coriell人類(lèi)基因(yīn)組(zǔ)DNA標準(zhǔn)品(GM05114)，歡迎選(xuǎn)購(gòu)！