Integrin alpha 8 recessive mutations are responsible for bilateral renal agenesis in humans

American Journal of Human Genetics

Volumn 94, Issue 2, 2014, Pages 288-294

  Humbert, Camille ^a,b   Silbermann, Flora ^a,b   Morar, Bharti ^c   Parisot, Mélanie ^a   Zarhrate, Mohammed ^a   Masson, Cécile ^b   Tores, Frédéric ^b   Blanchet, Patricia ^d   Perez, Marie José ^d   Petrov, Yuliya ^e   Khau Van Kien, Philippe ^e   Roume, Joelle ^f   Leroy, Brigitte ^f   Gribouval, Olivier ^a,b   Kalaydjieva, Luba ^c   Heidet, Laurence ^a   Salomon, Rémi ^a,b   Antignac, Corinne ^a,b   Benmerah, Alexandre ^a,b   Saunier, Sophie ^a,b   Jeanpierre, Cécile ^a,b   more..

^a HÔPITAL NECKER ENFANTS MALADES   (France)

^b UNIVERSITÉ PARIS DESCARTES   (France)

^c UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

^d HÔPITAL ARNAUD DE VILLENEUVE   (France)

^e DEPARTMENT OF NEUROLOGY   (France)

^f CENTRE HOSPITALIER INTERCOMMUNAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CONGENITAL ABNORMALITIES; FEMALE; FETUS; GENES, RECESSIVE; HOMOZYGOTE; HUMANS; INTEGRIN ALPHA CHAINS; KIDNEY; KIDNEY DISEASES; MALE; MUTATION; PEDIGREE; UROGENITAL ABNORMALITIES;

EID: 84893811998     PISSN: 00029297     EISSN: 15376605     Source Type: Journal    
DOI: 10.1016/j.ajhg.2013.12.017     Document Type: Article

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