PMID- 11102994
OWN - NLM
STAT- MEDLINE
DCOM- 20010111
LR  - 20131121
IS  - 1098-1004 (Electronic)
IS  - 1059-7794 (Linking)
VI  - 16
IP  - 6
DP  - 2000 Dec
TI  - A novel mutation E179K of the MEN1 gene predisposes for multiple endocrine 
      neoplasia-type 1 (MEN1).
PG  - 533
FAU - Weinhaeusel, A
AU  - Weinhaeusel A
AD  - Children's Cancer Research Institute, St Anna Children's Hospital, 
      Kinderspitalgasse 6, A-1090 Vienna, Austria. wienhausl@ccri.univie.ac.at
FAU - Vierhapper, H
AU  - Vierhapper H
FAU - Schlegl, R
AU  - Schlegl R
FAU - Wagner, T
AU  - Wagner T
FAU - Muhr, D
AU  - Muhr D
FAU - Scheuba, C
AU  - Scheuba C
FAU - Niederle, B
AU  - Niederle B
FAU - Haas, O A
AU  - Haas OA
LA  - eng
PT  - Journal Article
PL  - United States
TA  - Hum Mutat
JT  - Human mutation
JID - 9215429
RN  - 3KX376GY7L (Glutamic Acid)
RN  - K3Z4F929H6 (Lysine)
SB  - IM
MH  - Adenoma/genetics
MH  - Adolescent
MH  - Adult
MH  - Amino Acid Substitution/*genetics
MH  - Diabetes Mellitus, Type 2/genetics
MH  - Genetic Predisposition to Disease/genetics
MH  - *Glutamic Acid
MH  - Humans
MH  - Hyperinsulinism/genetics
MH  - Hyperparathyroidism/genetics
MH  - Insulinoma/genetics
MH  - *Lysine
MH  - Male
MH  - Multiple Endocrine Neoplasia Type 1/*genetics
MH  - Mutation, Missense/*genetics
MH  - Nuclear Family
MH  - Pancreatic Neoplasms/genetics
EDAT- 2000/01/11 19:15
MHDA- 2001/02/28 10:01
CRDT- 2000/01/11 19:15
PHST- 2000/01/11 19:15 [pubmed]
PHST- 2001/02/28 10:01 [medline]
PHST- 2000/01/11 19:15 [entrez]
AID - 10.1002/1098-1004(200012)16:6<533::AID-HUMU22>3.0.CO;2-5 [pii]
AID - 10.1002/1098-1004(200012)16:6<533::AID-HUMU22>3.0.CO;2-5 [doi]
PST - ppublish
SO  - Hum Mutat. 2000 Dec;16(6):533. doi: 
      10.1002/1098-1004(200012)16:6<533::AID-HUMU22>3.0.CO;2-5.