Results
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Screening of the LIX1 gene in Japanese and Malaysian patients with SMA and/or SMA-like disorder. [electronic resource] by
- Sasongko, Teguh Haryo
- Yusoff, Surini
- Atif, Amin Baig
- Fatemeh, Hayati
- Rani, Abdulqawee
- Marini, Marzuki
- Ab Aziz, Che Badariah
- Zabidi-Hussin, Z A M H
- Nishio, Hisahide
- Zilfalil, Bin Alwi
Producer: 20100624
In:
Brain & development vol. 32
Availability: No items available.
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644.
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645.
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646.
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647.
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648.
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649.
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650.
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651.
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Pathological impact of SMN2 mis-splicing in adult SMA mice. [electronic resource] by
- Sahashi, Kentaro
- Ling, Karen K Y
- Hua, Yimin
- Wilkinson, John Erby
- Nomakuchi, Tomoki
- Rigo, Frank
- Hung, Gene
- Xu, David
- Jiang, Ya-Ping
- Lin, Richard Z
- Ko, Chien-Ping
- Bennett, C Frank
- Krainer, Adrian R
Producer: 20140603
In:
EMBO molecular medicine vol. 5
Availability: No items available.
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652.
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653.
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655.
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657.
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658.
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659.
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Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy. [electronic resource] by
- Mendell, Jerry R
- Al-Zaidy, Samiah
- Shell, Richard
- Arnold, W Dave
- Rodino-Klapac, Louise R
- Prior, Thomas W
- Lowes, Linda
- Alfano, Lindsay
- Berry, Katherine
- Church, Kathleen
- Kissel, John T
- Nagendran, Sukumar
- L'Italien, James
- Sproule, Douglas M
- Wells, Courtney
- Cardenas, Jessica A
- Heitzer, Marjet D
- Kaspar, Allan
- Corcoran, Sarah
- Braun, Lyndsey
- Likhite, Shibi
- Miranda, Carlos
- Meyer, Kathrin
- Foust, K D
- Burghes, Arthur H M
- Kaspar, Brian K
Producer: 20171109
In:
The New England journal of medicine vol. 377
Availability: No items available.
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660.
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Complete sequencing of the SMN2 gene in SMA patients detects SMN gene deletion junctions and variants in SMN2 that modify the SMA phenotype. [electronic resource] by
- Ruhno, Corey
- McGovern, Vicki L
- Avenarius, Matthew R
- Snyder, Pamela J
- Prior, Thomas W
- Nery, Flavia C
- Muhtaseb, Abdurrahman
- Roggenbuck, Jennifer S
- Kissel, John T
- Sansone, Valeria A
- Siranosian, Jennifer J
- Johnstone, Alec J
- Nwe, Pann H
- Zhang, Ren Z
- Swoboda, Kathryn J
- Burghes, Arthur H M
Producer: 20190325
In:
Human genetics vol. 138
Availability: No items available.
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