TY  - GEN
AU  - Jin,Xin
AU  - Chen,Lanlan
AU  - Wang,Dajiang
AU  - Zhang,Yixin
AU  - Chen,Zehua
AU  - Huang,Houbin
TI  - Novel compound heterozygous mutation in the POC1B gene underlie peripheral cone dystrophy in a Chinese family
SN  - 1744-5094
PY  - 2019///0410
KW  - Adult
KW  - Asian People
KW  - genetics
KW  - Cell Cycle Proteins
KW  - Cone-Rod Dystrophies
KW  - Female
KW  - Heterozygote
KW  - Humans
KW  - Male
KW  - Mutation
KW  - Pedigree
KW  - Retinitis Pigmentosa
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1080/13816810.2018.1430239
ER  -