Keutel syndrome: Report of two novel MGP mutations and discussion of clinical overlap with arylsulfatase E deficiency and relapsing polychondritis
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K. Sund | R. Hopkin | Jinoh Kim | D. del Gaudio | S. Boyadjiev | M. Henrickson | M. Bober | K. Weaver | G. Acar | A. Yuksel | Simeon A. Boyadjiev | Moussa El Hallek | Kristen L. Sund