Kwan, B., Champion, B., Boyages, S., Munns, C. F., Clifton-Bligh, R., Luxford, C., & Crawford, B. (2018). A novel CASR mutation (p.Glu757Lys) causing autosomal dominant hypocalcaemia type 1. Endocrinol Diabetes Metab Case Rep.

Kwan, Benjamin, Bernard Champion, Steven Boyages, Craig F. Munns, Roderick Clifton-Bligh, Catherine Luxford, و Bronwyn Crawford. "A Novel CASR Mutation (p.Glu757Lys) Causing Autosomal Dominant Hypocalcaemia Type 1." Endocrinol Diabetes Metab Case Rep 2018.

Kwan, Benjamin, et al. "A Novel CASR Mutation (p.Glu757Lys) Causing Autosomal Dominant Hypocalcaemia Type 1." Endocrinol Diabetes Metab Case Rep 2018.