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1 Ergebnisse
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A nonsense CC2D1A variant is associated with congenital ano..:
Yi, Sheng
;
Tang, Xianglian
;
Zhang, Qiang
...
Heliyon. 10 (2024) 6 - p. e27946 , 2024
Link:
https://doi.org/10.1016/j.heliyon.2024.e27946
RT Journal T1
A nonsense CC2D1A variant is associated with congenital anomalies, motor delay, hypotonia, and slight deformities
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.heliyon.2024.e27946&Exemplar=1&LAN=DE A1 Yi, Sheng A1 Tang, Xianglian A1 Zhang, Qiang A1 Liang, Yu A1 Huang, Jing A1 Zhang, Shujie A1 Huang, Limei A1 Yi, Shang A1 Huang, Minpan A1 Qin, Zailong A1 Luo, Jingsi PB Elsevier BV YR 2024 SN 2405-8440 JF Heliyon VO 10 IS 6 SP e27946 LK http://dx.doi.org/https://doi.org/10.1016/j.heliyon.2024.e27946 DO https://doi.org/10.1016/j.heliyon.2024.e27946 SF ELIB - SuUB Bremen
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