z-logo
Premium
Combined deficiency of factors V and VIII by chance coinheritance of parahaemophilia and haemophilia A, but not by mutations of either LMAN1 or MCFD2, in a Japanese family
Author(s) -
Suzuki S.,
Nakamura Y.,
Suzuki N.,
Yamazaki T.,
Takagi Y.,
Tamura S.,
Takagi A.,
Kanematsu T.,
Matsushita T.,
Kojima T.
Publication year - 2018
Publication title -
haemophilia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.213
H-Index - 92
eISSN - 1365-2516
pISSN - 1351-8216
DOI - 10.1111/hae.13360
Subject(s) - medicine , clinical science , library science , family medicine , alternative medicine , pathology , cancer pain , computer science

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom