Mutations in ARL2BP, a protein required for ciliary microtubule structure, cause syndromic male infertility in humans and mice

Cilia are evolutionarily conserved hair-like structures with a wide spectrum of key biological roles, and their dysfunction has been linked to a growing class of genetic disorders, known collectively as ciliopathies. Many strides have been made towards deciphering the molecular causes for these dise...

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Detalhes bibliográficos
Autor principal: Moye, Abigail R. (author)
Outros Autores: Bedoni, Nicola (author), Cunningham, Jessica G. (author), Sanzhaeva, Urikhan (author), Tucker, Eric S. (author), Mathers, Peter (author), Peter, Virginie G. (author), Quinodoz, Mathieu (author), Paris, Liliana P. (author), Coutinho-Santos, Luísa (author), Camacho, Pedro (author), Purcell, Madeleine G. (author), Winkelmann, Abbie C. (author), Foster, James A. (author), Pugacheva, Elena N. (author), Rivolta, Carlo (author), Ramamurthy, Visvanathan (author)
Formato: article
Idioma:eng
Publicado em: 2019
Assuntos:
Genetics
ARL2BP
Infertility
Texto completo:http://hdl.handle.net/10400.21/10524
País:Portugal
Oai:oai:repositorio.ipl.pt:10400.21/10524

Texto Completo

http://hdl.handle.net/10400.21/10524

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