A homozygous B3GAT3 mutation causes a severe syndrome with multiple fractures, expanding the phenotype of linkeropathy syndromes

Publisher： John Wiley & Sons Inc

E-ISSN： 1552-4833|167|11|2691-2696

ISSN： 1552-4825

Source： American Journal Of Medical Genetics Part A, Vol.167, Iss.11, 2015-11, pp. : 2691-2696

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