Molecular genetic study of a Japanese family with Lesch-Nyhan syndrome: a point mutation at the consensus region of RNA splicing (HPRTKeio).
Yamada, Y
Molecular genetic study of a Japanese family with Lesch-Nyhan syndrome: a point mutation at the consensus region of RNA splicing (HPRTKeio). [electronic resource] - The Japanese journal of human genetics Dec 1993 - 413-9 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0916-8478
10.1007/BF01907988 doi
Base Sequence
DNA Primers
Female
Humans
Hypoxanthine Phosphoribosyltransferase--deficiency
Japan
Lesch-Nyhan Syndrome--ethnology
Male
Molecular Sequence Data
Point Mutation
RNA Splicing
Molecular genetic study of a Japanese family with Lesch-Nyhan syndrome: a point mutation at the consensus region of RNA splicing (HPRTKeio). [electronic resource] - The Japanese journal of human genetics Dec 1993 - 413-9 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0916-8478
10.1007/BF01907988 doi
Base Sequence
DNA Primers
Female
Humans
Hypoxanthine Phosphoribosyltransferase--deficiency
Japan
Lesch-Nyhan Syndrome--ethnology
Male
Molecular Sequence Data
Point Mutation
RNA Splicing