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Two novel mutations involved in hereditary tyrosinemia type I.
- Source :
-
Human molecular genetics [Hum Mol Genet] 1995 Feb; Vol. 4 (2), pp. 319-20. - Publication Year :
- 1995
- Subjects :
- Adolescent
Amino Acid Sequence
Base Sequence
Blotting, Western
Canada
DNA analysis
Exons
Female
Humans
Hydrolases deficiency
Infant, Newborn
Liver chemistry
Male
Molecular Sequence Data
Norway
Peptides analysis
Polymerase Chain Reaction
Sequence Analysis, DNA
Tyrosine metabolism
Amino Acid Metabolism, Inborn Errors genetics
Hydrolases genetics
Mutation
Tyrosine blood
Tyrosine genetics
Subjects
Details
- Language :
- English
- ISSN :
- 0964-6906
- Volume :
- 4
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Human molecular genetics
- Publication Type :
- Academic Journal
- Accession number :
- 7757089
- Full Text :
- https://doi.org/10.1093/hmg/4.2.319