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1 . Academic Journal
Using coding and non-coding rare variants to target candidate genes in patients with severe tinnitus
저자
by
Alvaro Gallego-Martinez
;
Alba Escalera-Balsera
;
Natalia Trpchevska
;
Paula Robles-Bolivar
;
Pablo Roman-Naranjo
, et al.
소스
npj Genomic Medicine, Vol 7, Iss 1, Pp 1-9 (2022)
Open Access (DOAJ)
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7 . Academic Journal
Rare Coding Variants in Patients with Non-Syndromic Vestibular Dysfunction
저자
by
Angelo Augusto M. Sumalde
;
Melissa A. Scholes
;
Olivia A. Kalmanson
;
Elizabeth A. Terhune
;
Lidia Frejo
, et al.
소스
Genes, Vol 14, Iss 4, p 831 (2023)
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7 . Academic Journal
Defective α‐tectorin may involve tectorial membrane in familial Meniere disease
저자
by
Pablo Roman‐Naranjo
;
Alberto M. Parra‐Perez
;
Alba Escalera‐Balsera
;
Andres Soto‐Varela
;
Alvaro Gallego‐Martinez
, et al.
소스
Clinical and Translational Medicine, Vol 12, Iss 6, Pp n/a-n/a (2022)
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7 . Academic Journal
Excess of Rare Missense Variants in Hearing Loss Genes in Sporadic Meniere Disease
저자
by
Alvaro Gallego-Martinez
;
Teresa Requena
;
Pablo Roman-Naranjo
;
Jose A. Lopez-Escamez
.
소스
Frontiers in Genetics, Vol 10 (2019)
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6 . Academic Journal
Systematic Review of Sequencing Studies and Gene Expression Profiling in Familial Meniere Disease
저자
by
Alba Escalera-Balsera
;
Pablo Roman-Naranjo
;
Jose Antonio Lopez-Escamez
.
소스
Genes, Vol 11, Iss 12, p 1414 (2020)
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5 .
A novel nonsense variant in the CENPP gene segregates in a Swiss family with autosomal dominant low-frequency sensorineural hearing loss
저자
by
Paula Robles-Bolivar
;
David Bächinger
;
Alberto M. Parra-Perez
;
Pablo Román-Naranjo
;
Alba Escalera-Balsera
, et al.
소스
European Journal of Human Genetics
. 30:1301-1305
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7 .
Ultrarare missense and frameshift variants in the TECTA gene may involve tectorial membrane in familial Meniere disease
저자
by
Pablo Román-Naranjo
;
Alberto M. Parra-Perez
;
Alba Escalera-Balsera
;
Andrés Soto-Varela
;
Alvaro Gallego-Martinez
, et al.
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7 .
Clinical and molecular genetics of Meniere disease
저자
by
Estrella Martinez-Gomez
;
Alvaro Gallego-Martinez
;
Pablo Roman-Naranjo
;
Jose A. Lopez-Escamez
.
소스
Medizinische Genetik
. 32:141-148
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6 .
Burden of Rare Variants in the OTOG Gene in Familial Meniere's Disease
저자
by
Paz Pérez-Vázquez
;
Pablo Roman-Naranjo
;
Angel Batuecas-Caletrio
;
Maria del Carmen Moleon
;
Jose A. Lopez-Escamez
, et al.
소스
Ear and hearing
. 41(6)
Full Text (LWW)
Scopus
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7 .
Rare Variants in theOTOGGene Are a Frequent Cause of Familial Meniere’s Disease
저자
by
Paz Pérez-Vázquez
;
Jose A. Lopez-Escamez
;
Pablo Roman-Naranjo
;
Juan Manuel Espinosa-Sanchez
;
Andrés Soto-Varela
, et al.
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