M. Laubriat-Bianchin

Transthyretin gene analysis in European patients with suspected familial amyloid polyneuropathy

D. Booth, A. Harding, P. Thomas, 1996, Neuromuscular Disorders.

Transthyretin gene analysis in European patients with suspected familial amyloid polyneuropathy.

D. Booth, A. Harding, P. Thomas, 1995 .

Mutations in the fibrinogen aalpha gene account for the majority of cases of congenital afibrinogenemia.

S. Antonarakis, C. Rossier, M. Morris, 2000, Blood.