Associated Papers
Molecular evolutionary and structural analysis of familial exudative vitreoretinopathy associated FZD4 gene.
Seemab S et al.
Bmc Evolutionary Biology, 2019
Novel human pathological mutations. Gene symbol: CLCN1. Disease: myotonia congenita, autosomal recessive.
Morales F et al.
Human Genetics, 2007
Novel human pathological mutations. Gene symbol: F8. Disease: haemophilia A.
Garcia-Lozano JR
Human Genetics, 2007
Novel human pathological mutations. Gene symbol: F8. Disease: haemophilia A.
Garcia-Lozano JR
Human Genetics, 2007
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