CLN8 disease caused by large genomic deletions

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CLN8 disease caused by large genomic deletions

BACKGROUND The presence of deletions can complicate genetic diagnosis of autosomal recessive disease. METHOD The DNA of patients was analyzed in a diagnostic setting. RESULTS We present three unrelated patients each carrying deletions that encompass the 37 kb CLN8 gene and discuss their phenotype. Two of the cases were hemizygous for a mutant allele - their deletions unmasked a mutation in ...

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ژورنال

عنوان ژورنال: Molecular Genetics & Genomic Medicine

سال: 2016

ISSN: 2324-9269

DOI: 10.1002/mgg3.263