Functional Characterization of the MYO6 Variant p.E60Q in Non-Syndromic Hearing Loss Patients

Functional Characterization of the MYO6 Variant p.E60Q in Non-Syndromic Hearing Loss Patients

<p dir="ltr">Hereditary hearing loss (HHL) is a common genetic disorder accounting for at least 60% of pre-lingual deafness in children, of which 70% is inherited in an autosomal recessive pattern. The long tradition of consanguinity among the Qatari population has increased the prev...

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Bibliographic Details
Main Author: Moza Alkowari (18288922) (author)
Other Authors: Meritxell Espino-Guarch (15430868) (author), Sahar Daas (18288925) (author), Doua Abdelrahman (17280667) (author), Waseem Hasan (17280670) (author), Navaneethakrishnan Krishnamoorthy (391608) (author), Abbirami Sathappan (12862993) (author), Patrick Sheehan (1980892) (author), Nicholas Panhuys (18288928) (author), Xavier Estivill (23803) (author), The Qatar Genome Program Research Consortium (14778616) (author)
Published: 2022
Subjects:
Chemical sciences
Inorganic chemistry
Organic chemistry
Physical chemistry
Theoretical and computational chemistry
sensorineural hearing loss
MYO6
whole-genome sequencing
zebrafish
hair cells
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