Variant C.394c>t in FGF3 is a Recurrent Cause of Profound Congenital Deafness in Slovak Roma

Maria Giertlova, Martin Mistrik, Petra Drencakova, Veronika Lopackova, Renata Zemjarova Mezenska, Katarina Cokasova, Michaela Urminska, Zuzana Zbonakova,Viktor Stranecky,Lenka Noskova

EUROPEAN JOURNAL OF HUMAN GENETICS（2023）

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Variant C.394c&gt;t in FGF3 is a Recurrent Cause of Profound Congenital Deafness in Slovak Roma

Variant C.394c>t in FGF3 is a Recurrent Cause of Profound Congenital Deafness in Slovak Roma