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pro vyhledávání: '"De Leenheer Els MR"'
Autor:
Swinnen Freya KR, Coucke Paul J, De Paepe Anne M, Symoens Sofie, Malfait Fransiska, Gentile Filomena V, Sangiorgi Luca, D'Eufemia Patrizia, Celli Mauro, Garretsen Ton JTM, Cremers Cor WRJ, Dhooge Ingeborg JM, De Leenheer Els MR
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 6, Iss 1, p 88 (2011)
Abstract Background Osteogenesis Imperfecta (OI) is a heritable connective tissue disorder mainly caused by mutations in the genes COL1A1 and COL1A2 and is associated with hearing loss in approximately half of the cases. The hearing impairment usuall
Externí odkaz:
https://doaj.org/article/820762343f68459d85108f52732e9bfb
