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簡(jiǎn)要描述：Galactosidase alpha is involved in the hydrolysis of terminal, non reducing alpha D galactose residues in alpha D galactosides, including galactose oligosaccharides, galactomannans and galactohydrolase. Defects in GLA are the cause of Fabry's disease (FD). FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, fe
產(chǎn)品型號(hào)：bsm-62171R廠商性質(zhì)：生產(chǎn)廠家更新時(shí)間：2025-03-03訪 問 量： 179產(chǎn)品分類
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