TY  - GEN
AU  - Legius,E
AU  - Baten,E
AU  - Stul,M
AU  - Marynen,P
AU  - Cassiman,J J
TI  - Sporadic late onset ornithine transcarbamylase deficiency in a boy with somatic mosaicism for an intragenic deletion
SN  - 0009-9163
PY  - 1990///1106
KW  - Amino Acid Metabolism, Inborn Errors
KW  - genetics
KW  - Ammonia
KW  - blood
KW  - Child, Preschool
KW  - Chromosome Deletion
KW  - DNA Probes
KW  - Humans
KW  - Male
KW  - Mosaicism
KW  - Ornithine Carbamoyltransferase
KW  - Ornithine Carbamoyltransferase Deficiency Disease
KW  - Restriction Mapping
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1111/j.1399-0004.1990.tb03565.x
ER  -