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EMC10 homozygous variant identified in a family with global..:
Umair, Muhammad
;
Ballow, Mariam
;
Asiri, Abdulaziz
...
Clinical Genetics. 98 (2020) 6 - p. 555-561 , 2020
Link:
https://doi.org/10.1111/cge.13842
RT Journal T1
EMC10 homozygous variant identified in a family with global developmental delay, mild intellectual disability, and speech delay
UL https://suche.suub.uni-bremen.de/peid=cr-10.1111_cge.13842&Exemplar=1&LAN=DE A1 Umair, Muhammad A1 Ballow, Mariam A1 Asiri, Abdulaziz A1 Alyafee, Yusra A1 al Tuwaijri, Abeer A1 Alhamoudi, Kheloud M. A1 Aloraini, Taghrid A1 Abdelhakim, Marwa A1 Althagafi, Azza Thamer A1 Kafkas, Senay A1 Alsubaie, Lamia A1 Alrifai, Muhammad Talal A1 Hoehndorf, Robert A1 Alfares, Ahmed A1 Alfadhel, Majid PB Wiley YR 2020 SN 0009-9163 SN 1399-0004 JF Clinical Genetics VO 98 IS 6 SP 555 OP 561 LK http://dx.doi.org/https://doi.org/10.1111/cge.13842 DO https://doi.org/10.1111/cge.13842 SF ELIB - SuUB Bremen
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