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Showing results 16 to 17 of 17

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Issue Date	Title	Journal Title
2010	The L441P mutation of cystic fibrosis transmembrane conductance regulator and its molecular pathogenic mechanisms in a Korean patient with cystic fibrosis	JOURNAL OF KOREAN MEDICAL SCIENCE
2019	The TECTA mutation R1890C is identified as one of the causes of genetic hearing loss: a case report	BMC MEDICAL GENETICS