LA, J., JC, S., AS, C., JA, H., A, M., & M, S. (1992). Familial amyloidotic polyneuropathy: A new transthyretin position 30 mutation (alanine for valine) in a family of German descent. Clinical genetics, 41(2), 70. https://doi.org/10.1111/j.1399-0004.1992.tb03635.x
Chicago Style (17th ed.) CitationLA, Jones, Skare JC, Cohen AS, Harding JA, Milunsky A, and Skinner M. "Familial Amyloidotic Polyneuropathy: A New Transthyretin Position 30 Mutation (alanine for Valine) in a Family of German Descent." Clinical Genetics 41, no. 2 (1992): 70. https://doi.org/10.1111/j.1399-0004.1992.tb03635.x.
MLA (9th ed.) CitationLA, Jones, et al. "Familial Amyloidotic Polyneuropathy: A New Transthyretin Position 30 Mutation (alanine for Valine) in a Family of German Descent." Clinical Genetics, vol. 41, no. 2, 1992, p. 70, https://doi.org/10.1111/j.1399-0004.1992.tb03635.x.
