@article{Ng:2021:10.1016/j.ajhg.2021.04.013,
author = {Ng, BG and Sosicka, P and Fenaille, F and Harroche, A and Vuillaumier-Barrot, S and Porterfield, M and Xia, Z-J and Wagner, S and Bamshad, MJ and Vergnes-Boiteux, M-C and Cholet, S and Dalton, S and Dell, A and Dupre, T and Fiore, M and Haslam, SM and Huguenin, Y and Kumagai, T and Kulik, M and McGoogan, K and Michot, C and Nickerson, DA and Pascreau, T and Borgel, D and Raymond, K and Warad, D and Flanagan-Steet, H and Steet, R and Tiemeyer, M and Seta, N and Bruneel, A and Freeze, HH},
doi = {10.1016/j.ajhg.2021.04.013},
journal = {AMERICAN JOURNAL OF HUMAN GENETICS},
pages = {1040--1052},
title = {A mutation in <i>SLC37A4</i> causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction},
url = {http://dx.doi.org/10.1016/j.ajhg.2021.04.013},
volume = {108},
year = {2021}
}

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TY  - JOUR
AU  - Ng,BG
AU  - Sosicka,P
AU  - Fenaille,F
AU  - Harroche,A
AU  - Vuillaumier-Barrot,S
AU  - Porterfield,M
AU  - Xia,Z-J
AU  - Wagner,S
AU  - Bamshad,MJ
AU  - Vergnes-Boiteux,M-C
AU  - Cholet,S
AU  - Dalton,S
AU  - Dell,A
AU  - Dupre,T
AU  - Fiore,M
AU  - Haslam,SM
AU  - Huguenin,Y
AU  - Kumagai,T
AU  - Kulik,M
AU  - McGoogan,K
AU  - Michot,C
AU  - Nickerson,DA
AU  - Pascreau,T
AU  - Borgel,D
AU  - Raymond,K
AU  - Warad,D
AU  - Flanagan-Steet,H
AU  - Steet,R
AU  - Tiemeyer,M
AU  - Seta,N
AU  - Bruneel,A
AU  - Freeze,HH
DO  - 10.1016/j.ajhg.2021.04.013
EP  - 1052
PY  - 2021///
SN  - 0002-9297
SP  - 1040
TI  - A mutation in <i>SLC37A4</i> causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction
T2  - AMERICAN JOURNAL OF HUMAN GENETICS
UR  - http://dx.doi.org/10.1016/j.ajhg.2021.04.013
UR  - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000658897400004&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=a2bf6146997ec60c407a63945d4e92bb
VL  - 108
ER  - 

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