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1 Ergebnisse
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P4HA1 mutations cause a unique congenital disorder of conne..:
Zou, Yaqun
;
Donkervoort, Sandra
;
Salo, Antti M.
...
Human Molecular Genetics. 26 (2017) 12 - p. 2207-2217 , 2017
Link:
https://doi.org/10.1093/hmg/ddx110
RT Journal T1
P4HA1 mutations cause a unique congenital disorder of connective tissue involving tendon, bone, muscle and the eye
UL https://suche.suub.uni-bremen.de/peid=cr-10.1093_hmg_ddx110&Exemplar=1&LAN=DE A1 Zou, Yaqun A1 Donkervoort, Sandra A1 Salo, Antti M. A1 Foley, A. Reghan A1 Barnes, Aileen M. A1 Hu, Ying A1 Makareeva, Elena A1 Leach, Meganne E. A1 Mohassel, Payam A1 Dastgir, Jahannaz A1 Deardorff, Matthew A. A1 Cohn, Ronald D. A1 DiNonno, Wendy O. A1 Malfait, Fransiska A1 Lek, Monkol A1 Leikin, Sergey A1 Marini, Joan C. A1 Myllyharju, Johanna A1 Bönnemann, Carsten G. PB Oxford University Press (OUP) YR 2017 SN 0964-6906 SN 1460-2083 JF Human Molecular Genetics VO 26 IS 12 SP 2207 OP 2217 LK http://dx.doi.org/https://doi.org/10.1093/hmg/ddx110 DO https://doi.org/10.1093/hmg/ddx110 SF ELIB - SuUB Bremen
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