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Mutations in dynein genes in patients affected by isolated non-syndromic asthenozoospermia

  • Published:2008-05-20 Issue:8 Volume:23 Page:1957-1962
  • ISSN:1460-2350
  • Container-title:Human Reproduction
  • language:en
  • Short-container-title:

Author:

Zuccarello D.,Ferlin A.,Cazzadore C.,Pepe A.,Garolla A.,Moretti A.,Cordeschi G.,Francavilla S.,Foresta C.

Publisher

Oxford University Press (OUP)

Subject

Obstetrics and Gynaecology,Rehabilitation,Reproductive Medicine

Reference34 articles.

1. Genetical and ultrastructural aspects of the immotile-cilia syndrome;Afzelius;Am J Hum Genet,1981

2. Evidence for autosomal dominant inheritance through the maternal line in a case of primary ciliary diskinesia;Alvarez González;Actas Urol Esp,2006

3. Gene deletions in an infertile man with sperm fibrous sheath dysplasia;Baccetti;Hum Reprod,2005

4. Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia;Bartoloni;Proc Natl Acad Sci USA,2002

5. A novel X-linked recessive mental retardation syndrome comprising macrocephaly and ciliary dysfunction is allelic to oral–facial–digital type I syndrome;Budny;Hum Genet,2006
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