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Marfan syndrome caused by a mutation inFBN1that gives rise to cryptic splicing and a 33 nucleotide insertion in the coding sequence

✍ Scribed by Sarah Hutchinson; Paul B. Wordsworth; Penny A. Handford


Book ID
106137410
Publisher
Springer
Year
2001
Tongue
English
Weight
106 KB
Volume
109
Category
Article
ISSN
0340-6717

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