Mutations of the retinal specific ATP binding transporter gene (ABCR) in a single family segregating both autosomal recessive retinitis pigmentosa RP19 and Stargardt disease: evidence of clinical heterogeneity at this locus (Q35432649)
Jump to navigation
Jump to search
scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Mutations of the retinal specific ATP binding transporter gene (ABCR) in a single family segregating both autosomal recessive retinitis pigmentosa RP19 and Stargardt disease: evidence of clinical heterogeneity at this locus |
scientific article |
Statements
1 reference
Mutations of the retinal specific ATP binding transporter gene (ABCR) in a single family segregating both autosomal recessive retinitis pigmentosa RP19 and Stargardt disease: evidence of clinical heterogeneity at this locus (English)
1 reference
Munnich A
1 reference
Rozet JM
1 reference
Gerber S
1 reference
Ghazi I
1 reference
Perrault I
1 reference
Ducroq D
1 reference
Souied E
1 reference
Cabot A
1 reference
Dufier JL
1 reference
Kaplan J
1 reference
1 reference
1 reference