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Wiley, Journal of Inherited Metabolic Disease, 3(43), p. 507-517, 2020

DOI: 10.1002/jimd.12207

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The 1‐<sup>13</sup>C galactose breath test in GALT deficient patients distinguishes NBS detected variant patients but does not predict outcome in classical phenotypes

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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