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1 Ergebnisse
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A MYH3 mutation identified for the first time in a Chinese ..:
Xu, Yang
;
Kang, Qing-Lin
;
Zhang, Zhen-Lin
Neuromuscular Disorders. 28 (2018) 5 - p. 456-462 , 2018
Link:
https://doi.org/10.1016/j.nmd.2018.03.002
RT Journal T1
A MYH3 mutation identified for the first time in a Chinese family with Sheldon-Hall syndrome (DA2B)
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.nmd.2018.03.002&Exemplar=1&LAN=DE A1 Xu, Yang A1 Kang, Qing-Lin A1 Zhang, Zhen-Lin PB Elsevier BV YR 2018 SN 0960-8966 JF Neuromuscular Disorders VO 28 IS 5 SP 456 OP 462 LK http://dx.doi.org/https://doi.org/10.1016/j.nmd.2018.03.002 DO https://doi.org/10.1016/j.nmd.2018.03.002 SF ELIB - SuUB Bremen
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