Associated Papers
Comprehensive molecular analysis of 61 Egyptian families with hereditary nonsyndromic hearing loss.
Budde BS et al.
Clinical Genetics, 2020
Two novel homozygous missense mutations identified in the BSND gene in Moroccan patients with Bartter's syndrome.
Elrharchi S et al.
International Journal of Pediatric Otorhinolaryngology, 2018
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