Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Eva Bahor"'
Publikováno v:
Zdravniški Vestnik, Vol 87, Iss 1-2 (2018)
Lowe syndrome is a rare X-linked multisystemic disorder, caused by mutation of the OCRL gene which encodes OCRL-1 protein. The disease is characterized by the triad of congenital cataracts, intellectual disability, and Fanconi-like proximal renal tub
Externí odkaz:
https://doaj.org/article/995a74cabaee484380ffbd8ec6f53b06
Publikováno v:
Slovenian Medical Journal. 87
Lowe syndrome is a rare X-linked multisystemic disorder, caused by mutation of the OCRL gene which encodes OCRL-1 protein. The disease is characterized by the triad of congenital cataracts, intellectual disability, and Fanconi-like proximal renal tub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c607d83af8b8ec8e613325439b3b43e
https://doi.org/10.6016/zdravvestn.2613
https://doi.org/10.6016/zdravvestn.2613