MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update

Publisher： John Wiley & Sons Inc

E-ISSN： 1098-1004|39|3|333-344

ISSN： 1059-7794

Source： HUMAN MUTATION, Vol.39, Iss.3, 2018-03, pp. : 333-344

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