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A single base-pair deletion in the WFS1 gene causes Wolfram syndrome.
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Cushing disease presenting as arthritis. J Pediatr Endocrinol Metab. 2010 Jun;23(6):603-5.
Kaur S, Kulkarni KP, Kochar IP.
Severe dietary protein sensitivity and hyperinsulinemic hypoglycemia in a patient with heterozygous mutation in HADH gene.J Pediatr Endocrinol Metab. 2010 Sep;23(9):953-5.
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Pamidronate for fibrous dysplasia due to McCune Albright Syndrome. Indian Pediatr. 2010 Jul;47(7):633-5
