Identification of the CFTR...

Identification of the CFTR p.Phe508Del founder mutation in the absence of a polythymidine 9T allele in a Hispanic patient

Dharajiya, N, Chisholm, KM, Dietz, L, Sue Richards, C, Kharrazi, M, Schrijver, I
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Volume:
83
Language:
english
Journal:
Clinical Genetics
DOI:
10.1111/cge.12012
Date:
June, 2013
File:
PDF, 575 KB
english, 2013
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