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A novel exon 17 deletion mutation of RPGRIP1 gene in two siblings with Leber congenital amaurosis.
A novel exon 17 deletion mutation of RPGRIP1 gene in two siblings with Leber congenital amaurosis.
2014
Takuro Fujimaki
Takahide Suzuki
Ai Yanagawa
Eisuke Arai
Keiko Fujiki
Yuko Wada
Akira Murakami
Keywords:
Anatomy
Exon
RPGRIP1 gene
deletion mutation
Biology
Genetics
Leber congenital amaurosis
Correction
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