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Results of search for 'au:"Gatfield, D P"'
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Authors
Dewar, R A
Gatfield, D P
Gordon, B A
Haust, M D
Topics
Adult
Amino Acid Metabolism, Inborn Errors
Ammonia
Cells, Cultured
Child
Citrulline
Dietary Proteins
Female
Fibroblasts
Humans
In Vitro Techniques
Male
Mitochondria
Ornithine
Oxidation-Reduction
Skin
Syndrome
analogs & derivatives
blood
drug therapy
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English
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1.
The hyperornithinemia, hyperammonemia, homocitrullinuria syndrome: an ornithine transport defect remediable with ornithine supplements.
[electronic resource]
by
Gordon, B A
Gatfield, D P
Haust, M D
Producer:
19871027
In:
Clinical and investigative medicine. Medecine clinique et experimentale
vol. 10
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2.
Hyperornithinemia-hyperammonemia-homocitrullinuria (HHH)-syndrome. Ultrastructural changes of mitochondria in cultured dermal fibroblasts of three patients.
[electronic resource]
by
Haust, M D
Dewar, R A
Gatfield, D P
Gordon, B A
Producer:
19970114
In:
Pathology, research and practice
vol. 192
Online resources:
Available from publisher's website
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