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Regional Features of Lattice Corneal Dystrophy Patients in Aichi Prefecture: An Analysis of the TGFBI Gene

✍ Scribed by Koji Hirano; Makoto Nakamura; Noriaki Yamamoto; Yoshihiro Hotta


Book ID
114044477
Publisher
Springer
Year
2002
Tongue
English
Weight
40 KB
Volume
46
Category
Article
ISSN
0021-5155

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Pattern of deletions of the dystrophin g
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We have analyzed 59 unrelated Mexican Duchenne/Becker muscular dystrophy patients (DMD/BMD) using PCR analysis of the 2 prone deletion regions in the DMD gene. Thirty one (52%) of the patients had a deletion of one or several of the exons. Most of the alterations (87%) were clustered in exons 44-52,