华中科技大学主页平台管理系统 KE TIE--英文主页-- Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a South American family.

KE TIE

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Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a South American family.

Release time:2024-05-20 Hits:

Indexed by: Journal paper

Journal: J Hum Genet.

Volume: 54

Issue: 11

Page Number: 660-4

Date of Publication: 2009-05-20

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