GJB2 mutations in Iranian Azeri population with autosomal recessive nonsyndromic hearing loss (ARNSHL): First report of c.238 C>A mutation in Iran
Abbaspour Rodbaneh, Ehsan, Panahi, Mohammad, Rahimi, Bahareh, Mokabber, Haleh, Farajollahi, Reza, Davarnia, Behzad
Published in Journal of clinical laboratory analysis (01.11.2021)
Published in Journal of clinical laboratory analysis (01.11.2021)
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De novo KAT6B mutation causes Say-Barber-Biesecker-Young-Simpson variant of Ohdo syndrome in an Iranian boy: a case report
Davarnia, Behzad, Panahi, Mohammad, Rahimi, Bahareh, Anari, Hassan, Farajollahi, Reza, Rodbaneh, Ehsan Abbaspour, Jeddi, Farhad
Published in Journal of medical case reports (05.01.2024)
Published in Journal of medical case reports (05.01.2024)
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Journal Article