Associated Papers
Novel mutations associated with inherited human calcium-sensing receptor disorders: A clinical genetic study.
García-Castaño A et al.
European Journal of Endocrinology, 2019
[Familial hypocalciuric hypercalcemia: a new mutation].
Ubetagoyena Arrieta M et al.
Anales De Pediatria (barcelona, Spain : 2003), 2011
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