TY  - GEN
AU  - Busquets,C
AU  - Coll,M J
AU  - Ribes,A
TI  - Evidence of a single origin for the most frequent mutation (R402W) causing glutaryl-CoA dehydrogenase deficiency: identification of 3 novel polymorphisms and haplotype definition
SN  - 1098-1004
PY  - 2000///0203
KW  - Amino Acid Substitution
KW  - Glutaryl-CoA Dehydrogenase
KW  - Haplotypes
KW  - Humans
KW  - Linkage Disequilibrium
KW  - Mutation
KW  - Oxidoreductases
KW  - deficiency
KW  - Oxidoreductases Acting on CH-CH Group Donors
KW  - Polymerase Chain Reaction
KW  - Polymorphism, Genetic
KW  - Polymorphism, Single-Stranded Conformational
KW  - Spain
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/(SICI)1098-1004(200002)15:2<207::AID-HUMU15>3.0.CO;2-F
ER  -