PMID- 10563488
OWN - NLM
STAT- MEDLINE
DCOM- 19991123
LR  - 20190816
IS  - 0009-9163 (Print)
IS  - 0009-9163 (Linking)
VI  - 56
IP  - 3
DP  - 1999 Sep
TI  - Adult-onset familial hypertrophic cardiomyopathy caused by a novel mutation,
      R694C, in the MYH7 gene.
PG  - 244-6
FAU - Andersen, P S
AU  - Andersen PS
FAU - Havndrup, O
AU  - Havndrup O
FAU - Bundgaard, H
AU  - Bundgaard H
FAU - Larsen, L A
AU  - Larsen LA
FAU - Vuust, J
AU  - Vuust J
FAU - Kjeldsen, K
AU  - Kjeldsen K
FAU - Christiansen, M
AU  - Christiansen M
LA  - eng
PT  - Letter
PT  - Research Support, Non-U.S. Gov't
PL  - Denmark
TA  - Clin Genet
JT  - Clinical genetics
JID - 0253664
RN  - EC 3.6.4.1 (Myosin Heavy Chains)
SB  - IM
MH  - Age of Onset
MH  - Aged
MH  - Cardiomyopathy, Hypertrophic/*genetics
MH  - Female
MH  - Humans
MH  - Male
MH  - *Mutation, Missense
MH  - Myosin Heavy Chains/*genetics
MH  - Pedigree
EDAT- 1999/11/24 00:00
MHDA- 1999/11/24 00:01
CRDT- 1999/11/24 00:00
PHST- 1999/11/24 00:00 [pubmed]
PHST- 1999/11/24 00:01 [medline]
PHST- 1999/11/24 00:00 [entrez]
AID - 10.1034/j.1399-0004.1999.560313.x [doi]
PST - ppublish
SO  - Clin Genet. 1999 Sep;56(3):244-6. doi: 10.1034/j.1399-0004.1999.560313.x.