10.1002/(sici)1096-8628(19970303)69:1<102::aid-ajmg20>3.0.co;2-s
Doi:
10.1002/(sici)1096-8628(19970303)69:1<102::aid-ajmg20>3.0.co;2-s
Title:
Identification of mutations in the CACNL1A3 gene in 13 families of Scandinavian origin having hypokalemic periodic paralysis and evidence of a founder effect in Danish families
Author:
Sillén, Anna; Sørensen, Troels; Kantola, Ilkka; Friis, Mogens Laue; Gustavson, Karl-Henrik; Wadelius, Claes
Year: 1997
Month: 03
Day: 03
Volume: 69
Issue: 1
First_page: 102
Last_page: 106
Journal:
American Journal of Medical Genetics
Issnp: 0148-7299
Issne: 1096-8628
Md5: eadb43323e648261974ef6b7b8ebf68f
Filesize: 139146
Timeadded: 2014-08-31 00:42:22
Journalid: 1083
Original Link: https://www.wenrao.com/i/3iYpwGLXQPCBemKYR
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