Počet záznamů: 1
Compound heterozygous CACNA1H mutations associated with severe congenital amyotrophy
SYS 0505495 LBL 01000a^^22220027750^450 005 20240103222128.1 014 $a 85065771983 $2 SCOPUS 014 $a 31070086 $2 PUBMED 014 $a 000467823400001 $2 WOS 017 $a 10.1080/19336950.2019.1614415 $2 DOI 100 $a 20190614d m y slo 03 ba 101 $a eng $d eng 102 $a US 200 1-
$a Compound heterozygous CACNA1H mutations associated with severe congenital amyotrophy 215 $a 9 s. 463 -1
$1 001 cav_un_epca*0327661 $1 011 $a 1933-6950 $e 1933-6969 $1 200 1 $a Channels $v Roč. 13, č. 1 (2019), s. 153-161 $1 210 $c Taylor & Francis 610 $a congenital amyotrophy 610 $a CACNA1H 610 $a mutations 610 $a calcium channel 610 $a Ca(v)3.2 channel 610 $a T-type channel 700 -1
$3 cav_un_auth*0375971 $4 070 $a Carter $b M. T. $y CA 701 -1
$3 cav_un_auth*0375972 $4 070 $a McMillan $b H. J. $y CA 701 -1
$3 cav_un_auth*0375973 $4 070 $a Tomin $b Andriy $p UOCHB-X $i Iontové kanály a jejich patologie $j Ion Channels and Diseases $k 270/27 $l 270/27 $w Chemical biology for life and diseases $y UA $T Ústav organické chemie a biochemie AV ČR, v. v. i. 701 -1
$3 cav_un_auth*0312431 $4 070 $a Weiss $b Norbert $p UOCHB-X $i Iontové kanály a jejich patologie $j Ion Channels and Diseases $k 270/27 $l 270/27 $w Chemical biology for life and diseases $y FR $z K $T Ústav organické chemie a biochemie AV ČR, v. v. i. 856 $9 RIV $u https://www.tandfonline.com/doi/full/10.1080/19336950.2019.1614415
Počet záznamů: 1