TY  - GEN
AU  - Fu,Lijun
AU  - Luo,Sushan
AU  - Cai,Shuang
AU  - Hong,Wenjing
AU  - Guo,Ying
AU  - Wu,Jinjin
AU  - Liu,Tingliang
AU  - Zhao,Chongbo
AU  - Li,Fen
AU  - Huang,Huimin
AU  - Huang,Meirong
AU  - Wang,Jian
TI  - Identification of LAMP2 Mutations in Early-Onset Danon Disease With Hypertrophic Cardiomyopathy by Targeted Next-Generation Sequencing
SN  - 1879-1913
PY  - 2017///0524
KW  - Adolescent
KW  - Age of Onset
KW  - Blotting, Western
KW  - Cardiomyopathy, Dilated
KW  - genetics
KW  - Cardiomyopathy, Hypertrophic
KW  - Case-Control Studies
KW  - Child
KW  - Child, Preschool
KW  - Codon, Nonsense
KW  - Female
KW  - Fluorescent Antibody Technique
KW  - Genotype
KW  - Glycogen Storage Disease Type IIb
KW  - High-Throughput Nucleotide Sequencing
KW  - Humans
KW  - Infant
KW  - Lysosomal-Associated Membrane Protein 2
KW  - Male
KW  - Muscle, Skeletal
KW  - metabolism
KW  - Mutation
KW  - Myocardium
KW  - Phenotype
KW  - Sequence Analysis, DNA
KW  - Wolff-Parkinson-White Syndrome
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/j.amjcard.2016.06.037
ER  -