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5421.
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5422.
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Mutation of ATF6 causes autosomal recessive achromatopsia. [electronic resource] by
- Ansar, Muhammad
- Santos-Cortez, Regie Lyn P
- Saqib, Muhammad Arif Nadeem
- Zulfiqar, Fareeha
- Lee, Kwanghyuk
- Ashraf, Naeem Mahmood
- Ullah, Ehsan
- Wang, Xin
- Sajid, Sundus
- Khan, Falak Sher
- Amin-ud-Din, Muhammad
- Smith, Joshua D
- Shendure, Jay
- Bamshad, Michael J
- Nickerson, Deborah A
- Hameed, Abdul
- Riazuddin, Saima
- Ahmed, Zubair M
- Ahmad, Wasim
- Leal, Suzanne M
Producer: 20151028
In:
Human genetics vol. 134
Availability: No items available.
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5423.
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5424.
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5425.
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5426.
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5427.
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5428.
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5429.
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5430.
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The multiple sclerosis visual pathway cohort: understanding neurodegeneration in MS. [electronic resource] by
- Martínez-Lapiscina, Elena H
- Fraga-Pumar, Elena
- Gabilondo, Iñigo
- Martínez-Heras, Eloy
- Torres-Torres, Ruben
- Ortiz-Pérez, Santiago
- Llufriu, Sara
- Tercero, Ana
- Andorra, Magi
- Roca, Marc Figueras
- Lampert, Erika
- Zubizarreta, Irati
- Saiz, Albert
- Sanchez-Dalmau, Bernardo
- Villoslada, Pablo
Producer: 20160307
In:
BMC research notes vol. 7
Availability: No items available.
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5431.
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5432.
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5433.
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5434.
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5435.
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Mutations in CACNA2D4 Cause Distinctive Retinal Dysfunction in Humans. [electronic resource] by
- Ba-Abbad, Rola
- Arno, Gavin
- Carss, Keren
- Stirrups, Kathleen
- Penkett, Christopher J
- Moore, Anthony T
- Michaelides, Michel
- Raymond, F Lucy
- Webster, Andrew R
- Holder, Graham E
Producer: 20160714
In:
Ophthalmology vol. 123
Availability: No items available.
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5436.
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5437.
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5438.
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5439.
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5440.
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