TY  - GEN
AU  - Joensuu,T
AU  - Hämäläinen,R
AU  - Yuan,B
AU  - Johnson,C
AU  - Tegelberg,S
AU  - Gasparini,P
AU  - Zelante,L
AU  - Pirvola,U
AU  - Pakarinen,L
AU  - Lehesjoki,A E
AU  - de la Chapelle,A
AU  - Sankila,E M
TI  - Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 3
SN  - 0002-9297
PY  - 2001///1018
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Base Sequence
KW  - Chromosomes, Human, Pair 3
KW  - Cloning, Molecular
KW  - Contig Mapping
KW  - Deafness
KW  - Expressed Sequence Tags
KW  - Female
KW  - Finland
KW  - Founder Effect
KW  - Gene Expression Profiling
KW  - Genetic Linkage
KW  - Haplotypes
KW  - Humans
KW  - Linkage Disequilibrium
KW  - Male
KW  - Membrane Proteins
KW  - chemistry
KW  - Molecular Sequence Data
KW  - Mutation
KW  - Pedigree
KW  - Protein Structure, Secondary
KW  - Protein Structure, Tertiary
KW  - RNA, Messenger
KW  - analysis
KW  - Retina
KW  - metabolism
KW  - Retinal Degeneration
KW  - Syndrome
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1086/323610
ER  -