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  2. Details for: SLC4A11 mutations in Fuchs endothelial corneal dystrophy.
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SLC4A11 mutations in Fuchs endothelial corneal dystrophy. [electronic resource]

By:
  • Vithana, Eranga N
Contributor(s):
  • Morgan, Patricio E
  • Ramprasad, Vedam
  • Tan, Donald T H
  • Yong, Victor H K
  • Venkataraman, Divya
  • Venkatraman, Anandalakshmi
  • Yam, Gary H F
  • Nagasamy, Soumittra
  • Law, Ricky W K
  • Rajagopal, Rama
  • Pang, Chi P
  • Kumaramanickevel, Govindsamy
  • Casey, Joseph R
  • Aung, Tin
Producer: 20080314Description: 656-66 p. digitalISSN:
  • 1460-2083
Subject(s):
  • Adult
  • Aged
  • Aged, 80 and over
  • Amino Acid Sequence
  • Amino Acid Substitution
  • Anion Transport Proteins -- genetics
  • Antiporters -- genetics
  • Asian People -- genetics
  • Case-Control Studies
  • Cohort Studies
  • Conserved Sequence
  • Female
  • Frameshift Mutation
  • Fuchs' Endothelial Dystrophy -- diagnosis
  • Gene Deletion
  • Genetic Testing
  • Heterozygote
  • Humans
  • Male
  • Middle Aged
  • Models, Molecular
  • Molecular Sequence Data
  • Mutation, Missense
  • Sequence Homology, Amino Acid
  • Statistics as Topic
Online resources:
  • Available from publisher's website
In: Human molecular genetics vol. 17
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Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't

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SLC4A11 mutations in Fuchs endothelial corneal dystrophy.

APA

Vithana E. N., Morgan P. E., Ramprasad V., Tan D. T. H., Yong V. H. K., Venkataraman D., Venkatraman A., Yam G. H. F., Nagasamy S., Law R. W. K., Rajagopal R., Pang C. P., Kumaramanickevel G., Casey J. R. & Aung T. (20080314). SLC4A11 mutations in Fuchs endothelial corneal dystrophy. : Human molecular genetics.

Chicago

Vithana Eranga N, Morgan Patricio E, Ramprasad Vedam, Tan Donald T H, Yong Victor H K, Venkataraman Divya, Venkatraman Anandalakshmi, Yam Gary H F, Nagasamy Soumittra, Law Ricky W K, Rajagopal Rama, Pang Chi P, Kumaramanickevel Govindsamy, Casey Joseph R and Aung Tin. 20080314. SLC4A11 mutations in Fuchs endothelial corneal dystrophy. : Human molecular genetics.

Harvard

Vithana E. N., Morgan P. E., Ramprasad V., Tan D. T. H., Yong V. H. K., Venkataraman D., Venkatraman A., Yam G. H. F., Nagasamy S., Law R. W. K., Rajagopal R., Pang C. P., Kumaramanickevel G., Casey J. R. and Aung T. (20080314). SLC4A11 mutations in Fuchs endothelial corneal dystrophy. : Human molecular genetics.

MLA

Vithana Eranga N, Morgan Patricio E, Ramprasad Vedam, Tan Donald T H, Yong Victor H K, Venkataraman Divya, Venkatraman Anandalakshmi, Yam Gary H F, Nagasamy Soumittra, Law Ricky W K, Rajagopal Rama, Pang Chi P, Kumaramanickevel Govindsamy, Casey Joseph R and Aung Tin. SLC4A11 mutations in Fuchs endothelial corneal dystrophy. : Human molecular genetics. 20080314.

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