The genetic basis of infertility in men.


Autoria(s): Bhasin, S.; Mallidis, Con; Ma, K.
Data(s)

2000

Resumo

Subfertility in men is a heterogeneous syndrome, its pathophysiology remaining unknown in the majority of affected men. A large number of genes and loci are associated with sterility in experimental animals, but the human homologues of most of these genes have not been characterized. A British study suggested that, in a large proportion of men with idiopathic infertility, the disorder is inherited as an autosomal recessive trait; this provocative hypothesis needs confirmation. Because normal germ cell development requires the temporally and spatially co-ordinated expression of a number of gene products at the hypothalamic, pituitary and testicular levels, it is safe to predict that a large number of autosomal, as well as X- and Y-linked, genes will probably be implicated in different subsets of male subfertility.

Identificador

http://pure.qub.ac.uk/portal/en/publications/the-genetic-basis-of-infertility-in-men(a0f5ba3e-52d0-4c78-8a63-55bbebb267b5).html

http://dx.doi.org/10.1053/beem.2000.0085

http://www.scopus.com/inward/record.url?scp=0034528884&partnerID=8YFLogxK

Idioma(s)

eng

Direitos

info:eu-repo/semantics/restrictedAccess

Fonte

Bhasin , S , Mallidis , C & Ma , K 2000 , ' The genetic basis of infertility in men. ' Baillière's best practice , vol 14(3) , no. 3 , pp. 363-388 . DOI: 10.1053/beem.2000.0085

Palavras-Chave #/dk/atira/pure/subjectarea/asjc/1300/1310 #Endocrinology #/dk/atira/pure/subjectarea/asjc/2700/2712 #Endocrinology, Diabetes and Metabolism
Tipo

article