Mutations in TULP1, NR2E3, and MFRP genes in Indian families with autosomal recessive retinitis pigmentosa

Molecular Vision

Volumn 18, Issue , 2012, Pages 1165-1174

  Kannabiran, Chitra ^a,c   Singh, Hardeep ^a,c   Sahini, Nishika ^a,c   Jalali, Subhadra ^b,c   Mohan, Gayathri ^a,c  

^a Hyderabad Eye Research Foundation   (India)

^b Smt Kannuri Santhamma Centre for Vitreoretinal diseases   (India)

^c L V PRASAD EYE INSTITUTE   (India)

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA;

ADOLESCENT; ADULT; ARTICLE; CHILD; CHROMOSOME 11; CHROMOSOME 15; CHROMOSOME 6; CLINICAL ARTICLE; DISEASE ASSOCIATION; EYE EXAMINATION; EYE FUNDUS; FEMALE; GENE; GENE DELETION; GENE MAPPING; GENE MUTATION; GENETIC SCREENING; GENETIC VARIABILITY; HOMOZYGOSITY; HUMAN; HUMAN CELL; INDIA; MALE; MFRP GENE; MISSENSE MUTATION; NIGHT BLINDNESS; NR2E3 GENE; PEDIGREE ANALYSIS; PRIORITY JOURNAL; RETINA CONE; RETINA DYSTROPHY; RETINA ROD; RETINITIS PIGMENTOSA; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; TULP1 GENE;

ADOLESCENT; ADULT; AMINO ACID SEQUENCE; BASE SEQUENCE; CASE-CONTROL STUDIES; CHILD; CONSANGUINITY; EYE PROTEINS; FEMALE; GENES, RECESSIVE; HOMOZYGOTE; HUMANS; INDIA; MALE; MEMBRANE PROTEINS; MOLECULAR SEQUENCE DATA; MUTATION; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; ORPHAN NUCLEAR RECEPTORS; PEDIGREE; RETINITIS PIGMENTOSA;

EID: 84863325414     PISSN: None     EISSN: 10900535     Source Type: Journal    
DOI: None     Document Type: Article

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