000 01586 a2200445 4500
005 20250518095149.0
264 0 _c20201214
008 202012s 0 0 eng d
022 _a2375-2548
024 7 _a10.1126/sciadv.aax0069
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSarkar, Saswata S
245 0 0 _aThe hypertrophic cardiomyopathy mutations R403Q and R663H increase the number of myosin heads available to interact with actin.
_h[electronic resource]
260 _bScience advances
_c04 2020
300 _aeaax0069 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
650 0 4 _aActins
_xchemistry
650 0 4 _aAlleles
650 0 4 _aAmino Acid Substitution
650 0 4 _aBinding Sites
650 0 4 _aCardiomyopathy, Hypertrophic
_xgenetics
650 0 4 _aGenetic Predisposition to Disease
650 0 4 _aHumans
650 0 4 _aModels, Molecular
650 0 4 _aMutation
650 0 4 _aMyocardial Contraction
_xgenetics
650 0 4 _aMyosins
_xchemistry
650 0 4 _aProtein Binding
650 0 4 _aProtein Conformation
650 0 4 _aStructure-Activity Relationship
650 0 4 _aVentricular Myosins
_xgenetics
700 1 _aTrivedi, Darshan V
700 1 _aMorck, Makenna M
700 1 _aAdhikari, Arjun S
700 1 _aPasha, Shaik N
700 1 _aRuppel, Kathleen M
700 1 _aSpudich, James A
773 0 _tScience advances
_gvol. 6
_gno. 14
_gp. eaax0069
856 4 0 _uhttps://doi.org/10.1126/sciadv.aax0069
_zAvailable from publisher's website
999 _c30852105
_d30852105