A de novo G+1 → a mutation at the α2(I) exon 16 splice...

Human Mutation 1993 Vol. 2; Iss. 5

A de novo G+1 → a mutation at the α2(I) exon 16 splice donor site causes skipping of exon 16 in the cDNA of one allele of an OI Type IV proband

Jane D. Filie, Bonnie M. Orrison, Qin Wang, Mary Beth Lewis, Joan C. Marini
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Volume:
2
Year:
1993
Language:
english
Pages:
9
DOI:
10.1002/humu.1380020510
File:
PDF, 839 KB
english, 1993
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