TY  - GEN
AU  - Landau,D
AU  - Shalev,H
AU  - Ohaly,M
AU  - Carmi,R
TI  - Infantile variant of Bartter syndrome and sensorineural deafness: a new autosomal recessive disorder
SN  - 0148-7299
PY  - 1996///0319
KW  - Adolescent
KW  - Arabs
KW  - Bartter Syndrome
KW  - congenital
KW  - Deafness
KW  - genetics
KW  - Female
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Male
KW  - Pedigree
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1002/ajmg.1320590411
ER  -