Functional analysis of myosin mutations that cause familial hypertrophic cardiomyopathy. (Q34169619)
scientific article
Language:
(P31) (Q13442814)
(P50) (Q29447012)
(P304) 3023-3030
(P407) (Q1860)
(P433) 6
(P478) 75
(P577) Tuesday, December 1, 1998
(P1104) 8
(P1433) (Q2032955)
(P1476) "Functional analysis of myosin mutations that cause familial hypertrophic cardiomyopathy" (language: en)
(P2093) O Roopnarine
(P2860) (Q28244969)
(Q39780104)
(Q37362212)
(Q36437978)
(Q24671028)
(Q40958307)
(Q28288865)
(Q34017547)
(Q24324826)
(Q28588233)
(Q33595083)
(Q40934940)
(Q24309554)
(Q28259888)
(Q41493794)
(Q41584513)
(Q34986230)
(Q33174333)
(Q33909960)
(Q35195188)
(Q24316399)
(Q28236892)
(Q24316488)
(Q36708559)
(Q34386835)
(Q36821490)
(Q27729777)
(Q28284626)
(Q24304076)
(Q41305578)
(Q39759066)
(Q39725939)
(Q36529647)
(Q28258622)
(Q24676505)
(Q33153444)
(Q44319774)
(Q44046528)
(Q35612541)
(Q51280493)
(Q40281953)
(Q29620585)
(Q73227806)
(Q72427679)
(Q26778412)
(Q69301402)
(Q72332123)
(Q58491161)
(Q70621616)
other details
description scientific article

External Links