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Journal Article
PLoS ONE, ISSN 1932-6203, 07/2018, Volume 13, Issue 7, pp. e0200789 - e0200789
Journal Article
Journal of Genetics, ISSN 0022-1333, 7/2018, Volume 97, Issue 3, pp. 589 - 609
Journal Article
Human Genetics, ISSN 0340-6717, 7/2018, Volume 137, Issue 6, pp. 471 - 478
Hereditary hearing impairment is a common sensory disorder that is genetically and phenotypically heterogeneous. In this study, we used a homozygosity mapping... 
Human Genetics | Gene Function | Autosomal recessive hearing impairment | Deafness | Biomedicine | LMX1A | Metabolic Diseases | Exome sequencing | Molecular Medicine | GENETIC-VARIATION | DREHER | DATABASE | EAR | GENETICS & HEREDITY | FRAMEWORK | GENERATION | MUTATIONS | EXPRESSION | Morphogenesis | Homeobox | Hearing | Phenotypes | Computed tomography | Ears & hearing | Sense organs | C-Terminus | Hearing impairment | Bioinformatics | Inner ear | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 06/2018, Volume 13, Issue 6, pp. e0199048 - e0199048
Journal Article