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Identification of compound heterozygous mutations inAP1B1le..:
Vornweg, J.
;
Gläser, S.
;
Ahmad‐Anwar, M.
...
British Journal of Dermatology. 184 (2021) 6 - p. 1190-1192 , 2021
Link:
https://doi.org/10.1111/bjd.19815
RT Journal T1 <Title>Identification of compound heterozygous mutations inAP1B1leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome</Title> UL https://suche.suub.uni-bremen.de/peid=cr-10.1111_bjd.19815&Exemplar=1&LAN=DE A1 Vornweg, J. A1 Gläser, S. A1 Ahmad‐Anwar, M. A1 Zimmer, A.D. A1 Kuhn, M. A1 Hörer, S. A1 Korenke, G.C. A1 Grothaus, J. A1 Ott, H. A1 Fischer, J. PB Oxford University Press (OUP) YR 2021 SN 0007-0963 SN 1365-2133 JF British Journal of Dermatology VO 184 IS 6 SP 1190 OP 1192 LK http://dx.doi.org/https://doi.org/10.1111/bjd.19815 DO https://doi.org/10.1111/bjd.19815 SF ELIB - SuUB Bremen
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