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Agricola

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Agricola

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Genetic profiles of non-syndromic severe-profound hearing loss in Chinese Hans by whole-exome sequencing.

• Authors : Liu Y; Department of Otorhinolaryngology, The Second People's Hospital of Hangzhou Yuhang District, Hangzhou 311121, China; Department of Otorhinolaryngology-Head and Neck Surgery, The First Affiliated Hospital Zhejiang University School of Medicine, Hangzhou 310003, China.

Subjects: Genetic Profile*; Connexin 26/Connexin 26/Connexin 26/*genetics ; Hearing Loss/Hearing Loss/Hearing Loss/*genetics

• Source: Gene [Gene] 2022 Apr 20; Vol. 819, pp. 146258. Date of Electronic Publication: 2022 Feb 01.Publisher: Elsevier/North-Holland Country of Publication: Netherlands NLM ID: 7706761 Publication Model: Print-Electronic Cited Medium: Internet

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Agricola

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Agricola

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Novel recessive PDZD7 biallelic mutations associated with hereditary hearing loss in a Chinese pedigree.

• Authors : Luo H; Department of Medical Genetics, Zhongshan School of Medicine, Sun Yat-sen University, China.; Hassan RN

Subjects: Genes, Recessive* ; Mutation*; Asian People/Asian People/Asian People/*genetics

• Source: Gene [Gene] 2019 Aug 15; Vol. 709, pp. 65-74. Date of Electronic Publication: 2019 May 23.Publisher: Elsevier/North-Holland Country of Publication: Netherlands NLM ID: 7706761 Publication Model: Print-Electronic Cited Medium: Internet

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Genetic basis of hearing loss in Spanish, Hispanic and Latino populations.

• Authors : Mittal R; Department of Otolaryngology, University of Miami Miller School of Medicine, Miami, FL, USA.; Patel AP

Subjects: Ethnicity/Ethnicity/Ethnicity/*genetics ; Genetic Predisposition to Disease/Genetic Predisposition to Disease/Genetic Predisposition to Disease/*genetics ; Hearing Loss/Hearing Loss/Hearing Loss/*genetics

• Source: Gene [Gene] 2018 Mar 20; Vol. 647, pp. 297-305. Date of Electronic Publication: 2018 Jan 10.Publisher: Elsevier/North-Holland Country of Publication: Netherlands NLM ID: 7706761 Publication Model: Print-Electronic Cited Medium: Internet

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A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family.

• Authors : Bakhchane A; Laboratoire de Génétique Moléculaire Humaine, Département de Recherche Scientifique, Institut Pasteur du Maroc, Casablanca, Morocco.; Charoute H

Subjects: Hearing Loss/Hearing Loss/Hearing Loss/*genetics ; Membrane Proteins/Membrane Proteins/Membrane Proteins/*genetics ; Mutation/Mutation/Mutation/*genetics

• Source: Gene [Gene] 2015 Dec 10; Vol. 574 (1), pp. 28-33. Date of Electronic Publication: 2015 Jul 28.Publisher: Elsevier/North-Holland Country of Publication: Netherlands NLM ID: 7706761 Publication Model: Print-Electronic Cited Medium: Internet

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Agricola

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