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Identification of disease‐causing variants in the EXOSC gen..:
Beheshtian, Maryam
;
Fattahi, Zohreh
;
Fadaee, Mahsa
...
Clinical Genetics. 95 (2019) 6 - p. 718-725 , 2019
Link:
https://doi.org/10.1111/cge.13549
RT Journal T1
Identification of disease‐causing variants in the EXOSC gene family underlying autosomal recessive intellectual disability in Iranian families
UL https://suche.suub.uni-bremen.de/peid=cr-10.1111_cge.13549&Exemplar=1&LAN=DE A1 Beheshtian, Maryam A1 Fattahi, Zohreh A1 Fadaee, Mahsa A1 Vazehan, Raheleh A1 Jamali, Payman A1 Parsimehr, Elham A1 Kamgar, Mahboubeh A1 Zonooz, Mehrshid Faraji A1 Mahdavi, Shokouh Sadat A1 Kalhor, Zahra A1 Arzhangi, Sanaz A1 Abedini, Seyedeh Sedigheh A1 Kermani, Farahnaz Sabbagh A1 Mojahedi, Faezeh A1 Kalscheuer, Vera M. A1 Ropers, Hans‐Hilger. A1 Kariminejad, Ariana A1 Najmabadi, Hossein A1 Kahrizi, Kimia PB Wiley YR 2019 SN 0009-9163 SN 1399-0004 JF Clinical Genetics VO 95 IS 6 SP 718 OP 725 LK http://dx.doi.org/https://doi.org/10.1111/cge.13549 DO https://doi.org/10.1111/cge.13549 SF ELIB - SuUB Bremen
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