Carnitine palmitoyltransferase II deficiency: structure of the gene and characterization of two novel disease-causing mutations.
Verderio, E
Carnitine palmitoyltransferase II deficiency: structure of the gene and characterization of two novel disease-causing mutations. [electronic resource] - Human molecular genetics Jan 1995 - 19-29 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0964-6906
10.1093/hmg/4.1.19 doi
Adult
Amino Acid Sequence
Animals
Base Sequence
Carnitine O-Palmitoyltransferase--deficiency
DNA
DNA Restriction Enzymes--metabolism
Exons
Humans
Introns
Molecular Sequence Data
Mutation
Polymerase Chain Reaction
RNA, Messenger--genetics
Sequence Alignment
Carnitine palmitoyltransferase II deficiency: structure of the gene and characterization of two novel disease-causing mutations. [electronic resource] - Human molecular genetics Jan 1995 - 19-29 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0964-6906
10.1093/hmg/4.1.19 doi
Adult
Amino Acid Sequence
Animals
Base Sequence
Carnitine O-Palmitoyltransferase--deficiency
DNA
DNA Restriction Enzymes--metabolism
Exons
Humans
Introns
Molecular Sequence Data
Mutation
Polymerase Chain Reaction
RNA, Messenger--genetics
Sequence Alignment