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Editorial Comment to p.Leu636Pro mutation is associated with cystic fibrosis transmembrane conductance regulator‐related disorders (congenital bilateral absence of vas deferens). (25th May 2015)
Record Type:
Journal Article
Title:
Editorial Comment to p.Leu636Pro mutation is associated with cystic fibrosis transmembrane conductance regulator‐related disorders (congenital bilateral absence of vas deferens). (25th May 2015)
Main Title:
Editorial Comment to p.Leu636Pro mutation is associated with cystic fibrosis transmembrane conductance regulator‐related disorders (congenital bilateral absence of vas deferens)