Author:
Claes Stephan,Aguirre Tania,Simosa Venancio,Bustos Tania,Lander Rafael,Piras Marta,Legius Eric,Cassiman Jean-Jacques,Raeymaekers Peter
Subject
Genetics (clinical),Genetics
Reference10 articles.
1. CRASH syndrome: Clinical spectrum of corpus callosum, hypoplasia, retardation, adducted thumbs, spastic paraparesis and hydrocephalus due to mutations in one single gene, L1;Fransen;Eur J Hum Genet,1995
2. Molecular structure and functional testing of human L1 CAM: An interspecies comparison;Hlavin;Genomics,1991
3. X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations in the L1 gene;Jouet;Nature Genet,1994
4. New domains of neural cell-adhesion molecule L1 implicated in X-linked hydrocephalus and MASA syndrome;Jouet;Am J Hum Genet,1995
5. X linked hydrocephalus and MASA syndrome;Kenwrick;J Med Genet,1996
Cited by
6 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献