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Publikováno v:
Journal of Evolution of Medical and Dental Sciences. 3:15184-15186
etc account for 15% of the cases.2 Lamellar ichthyosis which is more common, is an autosomal recessive condition caused by mutations in the transglutaminase-1 gene, defect on chromosome 14q11.Lid ectropion and ocular complications like exposure kerat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a7b5a1f082f09ac573c623f38c10458
https://doi.org/10.14260/jemds/2014/4040
https://doi.org/10.14260/jemds/2014/4040
