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1 Ergebnisse
1
Novel PTCH1 mutation in Gorlin–Goltz syndrome potentially a..:
Gao, Qian
;
Xu, Nuo
;
Yang, Chengcan
..
Oral Diseases. 27 (2020) 3 - p. 475-483 , 2020
Link:
https://doi.org/10.1111/odi.13586
RT Journal T1
Novel PTCH1 mutation in Gorlin–Goltz syndrome potentially altered interactions with lipid bilayer
UL https://suche.suub.uni-bremen.de/peid=cr-10.1111_odi.13586&Exemplar=1&LAN=DE A1 Gao, Qian A1 Xu, Nuo A1 Yang, Chengcan A1 Yang, Kai A1 Bian, Zhuan PB Wiley YR 2020 SN 1354-523X SN 1601-0825 JF Oral Diseases VO 27 IS 3 SP 475 OP 483 LK http://dx.doi.org/https://doi.org/10.1111/odi.13586 DO https://doi.org/10.1111/odi.13586 SF ELIB - SuUB Bremen
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