PMID- 10394939
OWN - NLM
STAT- MEDLINE
DCOM- 19990723
LR  - 20190722
IS  - 0340-6717 (Print)
IS  - 0340-6717 (Linking)
VI  - 104
IP  - 5
DP  - 1999 May
TI  - Gene symbol: AGXT. Disease: primary hyperoxaluria type I.
PG  - 441
FAU - Amoroso, A
AU  - Amoroso A
AD  - Servizio di genetica medica, Istituto per l'infanzia burlo garofolo, Trieste,
      Italy.
FAU - Pirulli, D
AU  - Pirulli D
FAU - Puzzer, D
AU  - Puzzer D
FAU - Ferri, L
AU  - Ferri L
FAU - Crovella, S
AU  - Crovella S
FAU - Ferrettini, C
AU  - Ferrettini C
FAU - Marangella, M
AU  - Marangella M
FAU - Mazzola, G
AU  - Mazzola G
FAU - Florian, F
AU  - Florian F
LA  - eng
PT  - Journal Article
PL  - Germany
TA  - Hum Genet
JT  - Human genetics
JID - 7613873
RN  - 0 (DNA Transposable Elements)
SB  - IM
MH  - Amino Acid Substitution
MH  - Base Sequence
MH  - DNA Transposable Elements
MH  - Humans
MH  - Hyperoxaluria, Primary/classification/*genetics
MH  - *Mutation
MH  - Mutation, Missense
MH  - Sequence Deletion
EDAT- 1999/07/08 00:00
MHDA- 1999/07/08 00:01
CRDT- 1999/07/08 00:00
PHST- 1999/07/08 00:00 [pubmed]
PHST- 1999/07/08 00:01 [medline]
PHST- 1999/07/08 00:00 [entrez]
AID - 10.1007/s004390050984 [doi]
PST - ppublish
SO  - Hum Genet. 1999 May;104(5):441. doi: 10.1007/s004390050984.