PMID- 10090906
OWN - NLM
STAT- MEDLINE
DCOM- 20000405
LR  - 20220317
IS  - 0002-9297 (Print)
IS  - 0002-9297 (Linking)
VI  - 64
IP  - 4
DP  - 1999 Apr
TI  - A novel NTRK1 mutation associated with congenital insensitivity to pain with
      anhidrosis.
PG  - 1207-10
FAU - Greco, A
AU  - Greco A
FAU - Villa, R
AU  - Villa R
FAU - Tubino, B
AU  - Tubino B
FAU - Romano, L
AU  - Romano L
FAU - Penso, D
AU  - Penso D
FAU - Pierotti, M A
AU  - Pierotti MA
LA  - eng
GR  - E.0568/TI_/Telethon/Italy
PT  - Letter
PT  - Research Support, Non-U.S. Gov't
PL  - United States
TA  - Am J Hum Genet
JT  - American journal of human genetics
JID - 0370475
RN  - EC 2.7.10.1 (Receptor, trkA)
SB  - IM
MH  - 3T3 Cells
MH  - Amino Acid Substitution/genetics
MH  - Animals
MH  - Base Sequence
MH  - Exons/genetics
MH  - Female
MH  - Hereditary Sensory and Autonomic Neuropathies/*genetics
MH  - Humans
MH  - Male
MH  - Mice
MH  - Pedigree
MH  - Point Mutation/*genetics
MH  - Receptor, trkA/chemistry/*genetics/metabolism
PMC - PMC1377845
EDAT- 1999/03/26 03:02
MHDA- 2001/07/04 10:01
CRDT- 1999/03/26 03:02
PHST- 1999/03/26 03:02 [pubmed]
PHST- 2001/07/04 10:01 [medline]
PHST- 1999/03/26 03:02 [entrez]
AID - AJHG980687 [pii]
AID - 10.1086/302319 [doi]
PST - ppublish
SO  - Am J Hum Genet. 1999 Apr;64(4):1207-10. doi: 10.1086/302319.