The R245X mutation of PCDH15 in Ashkenazi Jewish children diagnosed with nonsyndromic hearing loss foreshadows retinitis pigmentosa

Zippora Brownstein, Tamar Ben-Yosef, Orit Dagan, Moshe Frydman, Dvorah Abeliovich, Michal Sagi, Fabian A. Abraham, Riki Taitelbaum-Swead, Mordechai Shohat, Minka Hildesheimer, Thomas B. Friedman, Karen B. Avraham*

*Corresponding author for this work

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Keyphrases

Biochemistry, Genetics and Molecular Biology

Medicine and Dentistry

Neuroscience