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Clinical Genetics, ISSN 0009-9163, 03/2018, Volume 93, Issue 3, pp. 682 - 686
Journal Article
Clinical Genetics, ISSN 0009-9163, 07/2016, Volume 90, Issue 1, pp. 90 - 95
Journal Article
Journal Article
Journal of Human Genetics, ISSN 1434-5161, 02/2013, Volume 58, Issue 2, pp. 102 - 108
Human hereditary deafness at the DFNB29 locus on chromosome 21q22.1 is caused by recessive mutations of CLDN14, encoding claudin 14. This tight junction... 
claudin 14 | Pakistan | mild hearing loss | profound deafness | CLDN14 | DFNB29 | FREQUENCIES | INNER-EAR | PROTEIN | STRIA VASCULARIS | GENE | FAMILIES | TIGHT-JUNCTION | GENETICS & HEREDITY | OCCLUDIN | RECESSIVE DEAFNESS DFNB29 | INTERCELLULAR-JUNCTIONS | Hearing Loss - genetics | Claudins - genetics | Phenotype | Pedigree | Humans | Female | Male | Mutation | Index Medicus
Journal Article
Journal of Cellular and Molecular Medicine, ISSN 1582-1838, 07/2011, Volume 15, Issue 7, pp. 1515 - 1527
Journal Article
Nature Genetics, ISSN 1061-4036, 11/2012, Volume 44, Issue 11, pp. 1265 - 1271
Journal Article
Journal Article
Journal Article