Počet záznamov: 1
Six novel mutations in the arginine vasopressin gene in 15 kindreds with autosomal dominant familial neurohypophyseal diabetes insipidus give further insight into the pathogenesis
SYS 0127712 LBL 00000naa^^22^^^^^^^^450 005 20160818134942.4 100 $a 20160818d2004 m y0sloy0103 ba 101 0-
$a eng 102 $a GB 200 1-
$a Six novel mutations in the arginine vasopressin gene in 15 kindreds with autosomal dominant familial neurohypophyseal diabetes insipidus give further insight into the pathogenesis $f Kovacs, L. ... [et al.] 303 $a Popis urobený z citácie 463 -1
$1 200 1 $a European journal of human genetics $v Vol. 12, no. 1 (2004), pp. 44–51 701 -1
$3 sllk_un_auth*p0026986 $a Kovács $b László $f 1950-2017 $p 2. detská klinika LF UK a DFNsP, Bratislava $4 070 701 -1
$3 sllk_un_auth*p0056370 $a Robertson $b G.L. 701 -1
$3 sllk_un_auth*p0037744 $a Gregersen $b N. $p Research Unit for Molecular Medicine, Clinical Institute, Aarhus University Hospital and Aarhus University $4 070 701 -1
$3 sllk_un_auth*p0056366 $a Rittig $b S. $p Department of pediatrics, Skejby university hospital, Aarhus, Dánsko $4 070 801 -0
$a SK $b BA006 $c 20160818 $g AACR2
Počet záznamov: 1