Cystic fibrosis transmembrane conductance regulator mutations in azoospermic and oligospermic men and their partners
To access this article, please choose from the options below
Sabina Gallati graduated in Biology and Genetics from the University of Berne. She has undertaken postdoctoral research and training in molecular genetics and forensics in London (UK), Würzburg (Germany), Boston (USA) and Quantico (USA) and has specialised in Medical Genetic Analysis. In 2003, she became Professor of Human Genetics and Head of the Division of Human Genetics at the Medical Faculty of the University of Berne. Her main research interests are genetic mechanisms in Cystic Fibrosis and CFTR-related disorders, hereditary haemochromatosis and mitochondriopathies. Dr Sabina Gallati
PII: S1472-6483(09)00066-2
doi:10.1016/j.rbmo.2009.09.002
© 2009 Reproductive Healthcare Ltd, Duck End Farm, Dry Drayton, Cambridge CB23 8DB, UK. Published by Elsevier Inc. All rights reserved.
