(Q27674852)
English
Bartter disease type 4b
Bartter disease that has material basis in simultaneous mutation in both the CLCNKA and CLCNKB genes
- BARTS4B
- Bartter syndrome, type 4b, digenic
- neonatal Bartter syndrome type 4B with sensorineural deafness
- BARTTER SYNDROME, TYPE 4B
- Bartter Syndrome, Infantile, With Sensorineural Deafness
Statements
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Identifiers
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