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Compound heterozygous TRPV4 mutations in two siblings with a complex phenotype including severe intellectual disability and neuropathy. [electronic resource] by
- Thibodeau, My Linh
- Peters, Colin H
- Townsend, Katelin N
- Shen, Yaoqing
- Hendson, Glenda
- Adam, Shelin
- Selby, Kathryn
- Macleod, Patrick M
- Gershome, Cynthia
- Ruben, Peter
- Jones, Steven J M
- Friedman, Jan M
- Gibson, William T
- Horvath, Gabriella A
Producer: 20180605
In:
American journal of medical genetics. Part A vol. 173
Availability: No items available.
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