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Missense mutation Leu72Pro located on the carboxyl terminal amphipathic helix of apolipoprotein C-II causes familial chylomicronemia syndrome
Ching-Wan Lam, Yuet-Ping Yuen, Wai-Fun Cheng, Yan-Wo Chan, Sui-Fan TongVolume:
364
Année:
2006
Langue:
english
Pages:
260
DOI:
10.1016/j.cca.2005.07.025
Fichier:
PDF, 254 KB
english, 2006