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Heimler Syndrome Is Caused by Hypomorphic Mutations in the ..:
Ratbi, Ilham
;
Falkenberg, Kim D.
;
Sommen, Manou
...
The American Journal of Human Genetics. 97 (2015) 4 - p. 535-545 , 2015
Link:
https://doi.org/10.1016/j.ajhg.2015.08.011
RT Journal T1
Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.ajhg.2015.08.011&Exemplar=1&LAN=DE A1 Ratbi, Ilham A1 Falkenberg, Kim D. A1 Sommen, Manou A1 Al-Sheqaih, Nada A1 Guaoua, Soukaina A1 Vandeweyer, Geert A1 Urquhart, Jill E. A1 Chandler, Kate E. A1 Williams, Simon G. A1 Roberts, Neil A. A1 El Alloussi, Mustapha A1 Black, Graeme C. A1 Ferdinandusse, Sacha A1 Ramdi, Hind A1 Heimler, Audrey A1 Fryer, Alan A1 Lynch, Sally-Ann A1 Cooper, Nicola A1 Ong, Kai Ren A1 Smith, Claire E.L. A1 Inglehearn, Christopher F. A1 Mighell, Alan J. A1 Elcock, Claire A1 Poulter, James A. A1 Tischkowitz, Marc A1 Davies, Sally J. A1 Sefiani, Abdelaziz A1 Mironov, Aleksandr A. A1 Newman, William G. A1 Waterham, Hans R. PB Elsevier BV YR 2015 SN 0002-9297 JF The American Journal of Human Genetics VO 97 IS 4 SP 535 OP 545 LK http://dx.doi.org/https://doi.org/10.1016/j.ajhg.2015.08.011 DO https://doi.org/10.1016/j.ajhg.2015.08.011 SF ELIB - SuUB Bremen
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