TY  - GEN
AU  - Finckh,U
AU  - Xu,S
AU  - Kumaramanickavel,G
AU  - Schürmann,M
AU  - Mukkadan,J K
AU  - Fernandez,S T
AU  - John,S
AU  - Weber,J L
AU  - Denton,M J
AU  - Gal,A
TI  - Homozygosity mapping of autosomal recessive retinitis pigmentosa locus (RP22) on chromosome 16p12.1-p12.3
SN  - 0888-7543
PY  - 1998///0608
KW  - Chromosome Mapping
KW  - Chromosomes, Human, Pair 16
KW  - Consanguinity
KW  - Crystallins
KW  - genetics
KW  - Genes, Recessive
KW  - Genetic Linkage
KW  - Haplotypes
KW  - Homozygote
KW  - Humans
KW  - Microsatellite Repeats
KW  - Pedigree
KW  - Retinitis Pigmentosa
KW  - mu-Crystallins
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1006/geno.1997.5194
ER  -