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pro vyhledávání: '"Arul, Sarvanan"'
Autor:
Samir Kumar, Praharaj, Mahima, Acharya, Arul, Sarvanan, Sreejayan, Kongasseri, Rishikesh V, Behere, P S V N, Sharma
Publikováno v:
Turk psikiyatri dergisi = Turkish journal of psychiatry. 23(3)
Usher syndrome (or Hallgren syndrome) is an autosomal recessive genetic disorder characterized by sensorineural deafness, retinitis pigmentosa, and variable vestibular deficit; Usher syndrome type II is the most common form. Various neuropsychiatric
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::40aa0e6ba3ff14539a027aaa6530c6f1
https://pubmed.ncbi.nlm.nih.gov/22949292
https://pubmed.ncbi.nlm.nih.gov/22949292
