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1 Ergebnisse
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Novel splice site mutation in EIF2AK3 gene causes Wolcott‐R..:
Al‐Aama, Jumana Yousuf
;
Al‐Zahrani, Hams Saeed
;
Jelani, Musharraf
...
Congenital Anomalies. 58 (2017) 1 - p. 39-40 , 2017
Link:
https://doi.org/10.1111/cga.12217
RT Journal T1
Novel splice site mutation in EIF2AK3 gene causes Wolcott‐Rallison syndrome in a consanguineous family from Saudi Arabia
UL https://suche.suub.uni-bremen.de/peid=cr-10.1111_cga.12217&Exemplar=1&LAN=DE A1 Al‐Aama, Jumana Yousuf A1 Al‐Zahrani, Hams Saeed A1 Jelani, Musharraf A1 Sabir, Hesham Salih A1 Al‐Saeedi, Saad Abdullah A1 Ahmed, Saleem PB Wiley YR 2017 SN 0914-3505 SN 1741-4520 JF Congenital Anomalies VO 58 IS 1 SP 39 OP 40 LK http://dx.doi.org/https://doi.org/10.1111/cga.12217 DO https://doi.org/10.1111/cga.12217 SF ELIB - SuUB Bremen
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