טוען...
Large genomic rearrangements in the CFTR gene contribute to CBAVD
BACKGROUND: By performing extensive scanning of whole coding and flanking sequences of the CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) gene, we had previously identified point mutations in 167 out of 182 (91.7%) males with isolated congenital bilateral absence of the vas deferens (CBA...
שמור ב:
Main Authors: | , , , , , , , |
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פורמט: | Artigo |
שפה: | Inglês |
יצא לאור: |
BioMed Central
2007
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נושאים: | |
גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1876208/ https://ncbi.nlm.nih.gov/pubmed/17448246 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-8-22 |
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