2017, Vol. 19(9): 968-974 DOI: 10.7499/j.issn.1008-8830.2017.09.007 | ||
Clinical features and MYO5B mutations of a family affected by microvillus inclusion disease | ||
CHENG Ying1, LIANG Hong2, CAI Na-Li3, GUO Li1, HUANG Yu-Ge3, SONG Yuan-Zong1 | ||
Department of Pediatrics, First Affiliated Hospital, Jinan University, Guangzhou 510630, China | ||
Received 2017-06-15 Revised 2017-07-26 | ||
Supporting info | ||