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Novel SLC4A11 mutations in patients with recessive congenital hereditary endothelial dystrophy (CHED2). Mutation in brief #958. Online. [electronic resource] by
- Ramprasad, Vedam L
- Ebenezer, Neil D
- Aung, Tin
- Rajagopal, Rama
- Yong, Victor H K
- Tuft, Stephen J
- Viswanathan, Deepa
- El-Ashry, Mohamed F
- Liskova, Petra
- Tan, Donald T H
- Bhattacharya, Shomi S
- Kumaramanickavel, Govindasamy
- Vithana, Eranga N
Producer: 20070621
In:
Human mutation vol. 28
Availability: No items available.
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16.
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The Mitochondrial Metallochaperone SCO1 Is Required to Sustain Expression of the High-Affinity Copper Transporter CTR1 and Preserve Copper Homeostasis. [electronic resource] by
- Hlynialuk, Christopher J
- Ling, Binbing
- Baker, Zakery N
- Cobine, Paul A
- Yu, Lisa D
- Boulet, Aren
- Wai, Timothy
- Hossain, Amzad
- El Zawily, Amr M
- McFie, Pamela J
- Stone, Scot J
- Diaz, Francisca
- Moraes, Carlos T
- Viswanathan, Deepa
- Petris, Michael J
- Leary, Scot C
Publication details: Cell reports Feb 2015
In:
Cell reports vol. 10
Availability: No items available.
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