To the editor

New England Journal of Medicine

Volumn 372, Issue 18, 2015, Pages 1769-

  Gillmore, Julian D ^a   Hawkins, Philip N ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; THREONINE; VALINE; PREALBUMIN;

BLACK PERSON; CAUCASIAN; GENE FREQUENCY; GENE MUTATION; GENETIC RISK; GENETIC VARIABILITY; HEART AMYLOIDOSIS; HUMAN; LETTER; POPULATION RESEARCH; PRIORITY JOURNAL; RACE DIFFERENCE; RISK FACTOR; WILD TYPE; AFRICAN AMERICAN; AMYLOIDOSIS; FEMALE; GENETICS; HEART FAILURE; MALE; RESTRICTIVE CARDIOMYOPATHY;

AFRICAN AMERICANS; AMYLOIDOSIS; CARDIOMYOPATHY, RESTRICTIVE; FEMALE; HEART FAILURE; HUMANS; MALE; PREALBUMIN;

EID: 84936772477     PISSN: 00284793     EISSN: 15334406     Source Type: Journal    
DOI: 10.1056/NEJMc1503222     Document Type: Letter

References (2)

1. 2013/14 NHS standard contract for diagnostic service for amyloidosis (all ages). NHS England, 2013 (http://www.england .nhs.uk/wp-content/uploads/2013/06/e13-diag-serv-amyloidosis .pdf).
2. Jacobson DR, Pastore RD, Yaghoubian R, et al. Variant-sequence transthyretin (isoleucine 122) in late-onset cardiac amyloidosis in black Americans. N Engl J Med 1997;336:466-73.