Erratum: Whole-exome sequencing reveals diverse modes of inheritance in sporadic mild to moderate sensorineural hearing loss in a pediatric population (Genetics in Medicine (2015) DOI: 10.1038/gim.2014.213);Whole-exome sequencing reveals diverse modes of inheritance in sporadic mild to moderate sensorineural hearing loss in a pediatric population

Genetics in Medicine

Volumn 17, Issue 11, 2015, Pages 901-911

  Kim, Nayoung K D ^a   Kim, Ah Reum ^b   Park, Kyung Tae ^b,c   Kim, So Young ^b   Kim, Min Young ^d   Nam, Jae Yong ^a,e   Woo, Se Jun ^d   Oh, Seung Ha ^b   Park, Woong Yang ^a,f   Choi, Byung Yoon ^d  

^a Samsung Medical Center   (South Korea)

^b Seoul National University   (South Korea)

^c Seoul ENT Clinic   (South Korea)

^d Seoul National University Bundang Hospital   (South Korea)

^e Samsung Advanced Institute of Technology (SAIT)   (South Korea)

^f Sungkyunkwan University   (South Korea)

Author keywords

Mild to moderate sensorineural hearing loss; nonsyndromic hearing impairment; whole exome sequencing

Indexed keywords

GPR98 PROTEIN; MYH14 PROTEIN; OTOGL PROTEIN; PDZ7 PROTEIN; PROTEIN; SERPINB6 PROTEIN; TECTA PROTEIN; UNCLASSIFIED DRUG; CONNEXIN 26; GAP JUNCTION PROTEIN;

ADOLESCENT; ADULT; ALLELE; ARTICLE; AUDITORY THRESHOLD; CHILDHOOD DISEASE; CONTROLLED STUDY; DISEASE SEVERITY; ENHANCER REGION; EXOME; EXON; FEMALE; GENE FREQUENCY; GENE MUTATION; GENETIC PROCEDURES; GENETIC VARIABILITY; HUMAN; INHERITANCE; MAJOR CLINICAL STUDY; MALE; PERCEPTION DEAFNESS; PHENOTYPE; SINGLE NUCLEOTIDE POLYMORPHISM; WHOLE EXOME SEQUENCING; X CHROMOSOME; AMINO ACID SEQUENCE; CHILD; COPY NUMBER VARIATION; DNA MUTATIONAL ANALYSIS; GENETICS; HEARING LOSS, SENSORINEURAL; HEARING TEST; HIGH THROUGHPUT SEQUENCING; INFANT; MOLECULAR GENETICS; MUTATION; NEWBORN; PEDIGREE; PRESCHOOL CHILD; SEQUENCE ALIGNMENT; SEVERITY OF ILLNESS INDEX;

ADOLESCENT; AMINO ACID SEQUENCE; CHILD; CHILD, PRESCHOOL; CONNEXINS; DNA COPY NUMBER VARIATIONS; DNA MUTATIONAL ANALYSIS; EXOME; FEMALE; HEARING LOSS, SENSORINEURAL; HEARING TESTS; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; INFANT; INFANT, NEWBORN; INHERITANCE PATTERNS; MALE; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; SEQUENCE ALIGNMENT; SEVERITY OF ILLNESS INDEX;

EID: 84947903023     PISSN: 10983600     EISSN: 15300366     Source Type: Journal    
DOI: 10.1038/gim.2015.122     Document Type: Erratum

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