Premium
LeaPIN’ toward the cause of myoglobinuria in childhood
Author(s) -
Brunham LR
Publication year - 2009
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.2008.01139_3.x
Subject(s) - myoglobinuria , medicine , rhabdomyolysis
Mutations in LPIN1 cause recurrent acute myoglobinuria in childhood
Zeharia et al. (2008)
The American Journal of Human Genetics 83: 1–6
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom