Mutation of perinatal myosin heavy chain (multiple letter) [4]

New England Journal of Medicine

Volumn 351, Issue 24, 2004, Pages 2556-2558

  Stratakis, Constantine A ^a   Bertherat, Jerome ^b   Carney, J Aidan ^c   Brown, Matthew A ^d   Morita, Hiroyuki ^e   Nagai, Ryozo ^e   Basson, Craig T ^f   Veugelers, Mark ^f   McDermott, Deborah A ^f  

^a NATIONAL INSTITUTES OF HEALTH   (United States)

^b Hôpital Cochin ^*  (France)

^c MAYO CLINIC   (United States)

^d UNIVERSITY OF OXFORD   (United Kingdom)

^e UNIVERSITY OF TOKYO   (Japan)

^f WEILL CORNELL MEDICAL COLLEGE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MYOSIN HEAVY CHAIN; MYH8 PROTEIN, HUMAN;

CARNEY COMPLEX; DNA POLYMORPHISM; GENE; GENE MUTATION; HUMAN; LENTIGO; LETTER; MYH8 GENE; MYXOMA; PRIORITY JOURNAL; ARTHROGRYPOSIS; CONGENITAL MALFORMATION; FINGER; GENETICS; MISSENSE MUTATION; NOTE; PIGMENT DISORDER; SYNDROME; TRISMUS; GENETIC POLYMORPHISM; HEART TUMOR; MUTATION; POPULATION GENETICS; HEART; PRENATAL DEVELOPMENT;

ARTHROGRYPOSIS; FINGERS; HUMANS; MUTATION, MISSENSE; MYOSIN HEAVY CHAINS; MYXOMA; PIGMENTATION DISORDERS; SYNDROME; TRISMUS; GENETICS, POPULATION; HEART NEOPLASMS; MUTATION; POLYMORPHISM, GENETIC; HEART;

EID: 13644275068     PISSN: 00284793     EISSN: None     Source Type: Journal    
DOI: 10.1056/NEJM200412093512420     Document Type: Letter

References (0)