term1 Definition1term2 Definition2term3 Definition3
Please sign in to your Google account to access your documents:
describe glutamine synthetase deficiency
extremely rare (only 2 cases)
consanguineous turkish parents
fatal (2 days and 4 weeks)
multiple symptoms
describe ornithine aminotransferase deficiency
error of ornithine metabolism
rare, autosomal recessive
myopia in childhood
night blindness
totally blind by 45-65 years old
describe effects of high levels of homocysteine
cardiovascular disease
Need help typing ? See our FAQ (opens in new window)
Please sign in to create this set. We'll bring you back here when you are done.
Discard Changes Sign in
Please sign in to add to folders.
Sign in
Don't have an account? Sign Up »
You have created 2 folders. Please upgrade to Cram Premium to create hundreds of folders!