Graham, U., Nesbit, M., Hannan, F., Howles, S., Thakker, R., & Hunter, S. (2013). Familial Hypocalciuric Hypercalcaemia Type 3 (FHH3) Identified in a Family in Northern Ireland Leading to Identification of a Causative Mutation in the Adaptor Protein 2 Sigma 1 (AP2S1) Gene.
Chicago-referens (17:e uppl.)Graham, U., M. Nesbit, F. Hannan, SA Howles, R. Thakker, och S. Hunter. Familial Hypocalciuric Hypercalcaemia Type 3 (FHH3) Identified in a Family in Northern Ireland Leading to Identification of a Causative Mutation in the Adaptor Protein 2 Sigma 1 (AP2S1) Gene. 2013.
MLA-referens (9:e uppl.)Graham, U., et al. Familial Hypocalciuric Hypercalcaemia Type 3 (FHH3) Identified in a Family in Northern Ireland Leading to Identification of a Causative Mutation in the Adaptor Protein 2 Sigma 1 (AP2S1) Gene. 2013.