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#613090 - BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS; BARTS4B
Cytogenetic locations: 1p36, 1p36
Gene summaries Genetic tests Medical literature
#607364 - BARTTER SYNDROME, TYPE 3; BARTS3
BARTTER SYNDROME, TYPE 3, WITH HYPOCALCIURIA, INCLUDED
Cytogenetic locations: 13333163
*602024 - CHLORIDE CHANNEL, KIDNEY, A; CLCNKA
Cytogenetic locations: 19326936
*602023 - CHLORIDE CHANNEL, KIDNEY, B; CLCNKB
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