Val2Ala mutation in the Atp6v0a4 gene causes early-onset sensorineural hearing loss in children with recessive distal renal tubular acidosis: a case report

✍ Scribed by Kose, Engin; Sirin Kose, Seda; Alparslan, Caner; Kasap Demir, Belde; Berdeli, Afig; Mutlubas Ozsan, Fatma; Yavascan, Onder; Aksu, Nejat

• Book ID: 121664913
• Publisher: Informa plc
• Year: 2014
• Tongue: English
• Weight: 283 KB
• Volume: 36
• Category: Article
• ISSN: 0886-022X
• DOI: 10.3109/0886022X.2014.890055