关键词: AIPL1 Leber congenital amaurosis cataract keratoconus mutation nystagmus
Mesh : Adaptor Proteins, Signal Transducing / genetics Child Child, Preschool Codon, Nonsense Female Humans Leber Congenital Amaurosis / genetics Male Pedigree Siblings
来 源:
DOI:10.1080/15513815.2019.1644687
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