Results 1 to 10 of about 9,773 (106)

Editorial: Genetics of non-syndromic hearing loss [PDF]

Frontiers in Genetics
Saba Battelino
exaly   +4 more sources

Autosomal Dominant Non-Syndromic Hearing Loss (DFNA): A Comprehensive Narrative Review [PDF]

Biomedicines, 2023
Salvatore Ferlito, Jérôme Lechien, Antonino Maniaci   +2 more
exaly   +2 more sources

Study Models for Non-Syndromic Hearing Loss. [PDF]

Cells
Hearing loss is the most common sensory disorder; It is estimated that nearly 2.5 billion people will have some degree of hearing loss by 2050. Although the causes are diverse, a significant proportion of cases have a genetic origin, which is the main focus of the models discussed in this review.
Hoyau V, Leclère JC, Moisan S.
europepmc   +5 more sources

TECTB Variants Reveal Tectorial Membrane Vulnerability in Dominant Non-Syndromic Hearing Loss. [PDF]

Adv Sci (Weinh)
Hale EB, Vona B, Goodyear RJ, Osgood RT, Shen J, Amr SS, Mojica K, Hofrichter MAH, Schröder J, Flandin S, Gratias P, Vera-Monroy R, Callahan K, Gudlewski KL, Quadros R, Ohtsuka M, McGee J, Walsh EJ, Morton CC, Haaf T, Gurumurthy C, Saunders JE, Richardson GP, Indzhykulian AA.   +23 more
europepmc   +1 more source

Negative Molecular Diagnostics in Non-Syndromic Hearing Loss: What Next? [PDF]

Genes (Basel), 2022
Clabout T, Maes L, Acke F, Wuyts W, Van Schil K, Coucke P, Janssens S, De Leenheer E.   +7 more
europepmc   +1 more source

Two Novel Compound Heterozygous <i>CDH23</i> Mutations Underlying Non-Syndromic Hearing Loss. [PDF]

Int J Gen Med
Xu P, Liao Q, Lin Y, Zhao N, Li L.
europepmc   +1 more source

Comprehensive Analysis and Genetic Insights Into GJB2 c.35delG Mutation-Associated Non-Syndromic Hearing Loss in Morocco. [PDF]

OTO Open
Salman EM, Qabli ME, Soufian L, Mansouri M, Bouzid FZ, Oulghoul O, Chehbouni M, Lakhdar Y, Rochdi Y, Raji A, Aboussair N.   +10 more
europepmc   +1 more source

Novel cis compound heterozygous variants in MYO6 causes early onset of non-syndromic hearing loss in a Chinese family. [PDF]

Front Genet, 2023
Ji H, Zhang L, Hussain HMJ, Aftab A, Yu H, Xiao M.   +5 more
europepmc   +1 more source

Identification of Novel <i>LOXHD1</i> Variants in Chinese Patients with Non-Syndromic Hearing Loss. [PDF]

J Otol
Zhang K, Xin X, Huang S, Hou B, Xu X, Qu P, Han X, Zhang H.   +7 more
europepmc   +1 more source

Molecular diagnosis of non-syndromic hearing loss in seven Iranian families using whole-exome sequencing. [PDF]

BMC Med Genomics
Abghari FZ, Esmaeilzadeh E, Biglari S, Ghasemi H, Mohseni M, Shahmohammad N, Khorshid HRK, Najafipour R.   +7 more
europepmc   +1 more source