Rare cases of galactose metabolic disorders: Identification of more than two mutations per patient

Citation:

Schulpis KH, Thodi G, Chatzidaki M, Iakovou K, Molou E, Dotsikas Y, Loukas YL. Rare cases of galactose metabolic disorders: Identification of more than two mutations per patient. Journal of Pediatric Endocrinology and Metabolism [Internet]. 2017;30:1119-1120.

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