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Novel homozygous ENPP1 mutation causes generalized arterial..:
Staretz‐Chacham, Orna
;
Shukrun, Rachel
;
Barel, Ortal
...
American Journal of Medical Genetics Part A. 179 (2019) 10 - p. 2112-2118 , 2019
Link:
https://doi.org/10.1002/ajmg.a.61334
RT Journal T1 <Title>Novel homozygous ENPP1 mutation causes generalized arterial calcifications of infancy, thrombocytopenia, and cardiovascular and central nervous system syndrome</Title> UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_ajmg.a.61334&Exemplar=1&LAN=DE A1 Staretz‐Chacham, Orna A1 Shukrun, Rachel A1 Barel, Ortal A1 Pode‐Shakked, Ben A1 Pleniceanu, Oren A1 Anikster, Yair A1 Shalva, Nechama A1 Ferreira, Carlos R. A1 Ben‐Haim Kadosh, Admit A1 Richardson, Justin A1 Mane, Shrikant M. A1 Hildebrandt, Friedhelm A1 Vivante, Asaf PB Wiley YR 2019 SN 1552-4825 SN 1552-4833 JF American Journal of Medical Genetics Part A VO 179 IS 10 SP 2112 OP 2118 LK http://dx.doi.org/https://doi.org/10.1002/ajmg.a.61334 DO https://doi.org/10.1002/ajmg.a.61334 SF ELIB - SuUB Bremen
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