De Novo ACTG1 Variant Expands the Phenotype and Genotype of Partial Deafness and Baraitser-Winter Syndrome

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Published in:International journal of molecular sciences 2022, Vol.23 (2)
Main Authors: Dawidziuk, Mateusz, Kutkowska-Kazmierczak, Anna, Bukowska-Olech, Ewelina, Jurek, Marta, Kalka, Ewa, Guilbride, Dorothy Lys, Furmanek, Mariusz Ireneusz, Bekiesinska-Figatowska, Monika, Bal, Jerzy, Gawlinski, Pawel
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container_title International journal of molecular sciences
container_volume 23
creator Dawidziuk, Mateusz
Kutkowska-Kazmierczak, Anna
Bukowska-Olech, Ewelina
Jurek, Marta
Kalka, Ewa
Guilbride, Dorothy Lys
Furmanek, Mariusz Ireneusz
Bekiesinska-Figatowska, Monika
Bal, Jerzy
Gawlinski, Pawel
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doi_str_mv 10.3390/ijms23020692
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title De Novo ACTG1 Variant Expands the Phenotype and Genotype of Partial Deafness and Baraitser-Winter Syndrome
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