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A missense mutation in the nuclear localization signal sequence of CERKL (p.R106S) causes autosomal recessive retinal degeneration. [electronic resource] by
- Ali, Manir
- Ramprasad, Vedam Lakshmi
- Soumittra, Nagasamy
- Mohamed, Moin D
- Jafri, Hussain
- Rashid, Yasmin
- Danciger, Michael
- McKibbin, Martin
- Kumaramanickavel, Govindasamy
- Inglehearn, Chris F
Producer: 20090306
In:
Molecular vision vol. 14
Availability: No items available.
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8.
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Identification of a novel splice-site mutation in the Lebercilin (LCA5) gene causing Leber congenital amaurosis. [electronic resource] by
- Ramprasad, Vedam Lakshmi
- Soumittra, Nagasamy
- Nancarrow, Derek
- Sen, Parveen
- McKibbin, Martin
- Williams, Grange A
- Arokiasamy, Tharigopala
- Lakshmipathy, Praveena
- Inglehearn, Chris F
- Kumaramanickavel, Govindasamy
Producer: 20080506
In:
Molecular vision vol. 14
Availability: No items available.
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9.
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CERKL mutations cause an autosomal recessive cone-rod dystrophy with inner retinopathy. [electronic resource] by
- Aleman, Tomas S
- Soumittra, Nagasamy
- Cideciyan, Artur V
- Sumaroka, Alexander M
- Ramprasad, Vedam Lakshmi
- Herrera, Waldo
- Windsor, Elizabeth A M
- Schwartz, Sharon B
- Russell, Robert C
- Roman, Alejandro J
- Inglehearn, Chris F
- Kumaramanickavel, Govindasamy
- Stone, Edwin M
- Fishman, Gerald A
- Jacobson, Samuel G
Producer: 20091223
In:
Investigative ophthalmology & visual science vol. 50
Availability: No items available.
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