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Migraine comorbidity: from genotype to phenotype

✍ Scribed by Guiseppe Nappi *, †, ‡ , Alfredo Costa *, ‡ , Daniela Fortini; Maria G. Damiano; Carlo Casali; Francesco Pierelli

Publisher
Springer
Year
2000
Tongue
English
Weight
51 KB
Volume
1
Category
Article
ISSN
1129-2369

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In 5-10% of patients, neurofibromatosis type 1 (NF1) results from microdeletions that encompass the entire NF1 gene and a variable number of flanking genes. Two recurrent microdeletion types are found in most cases, with microdeletion breakpoints located in paralogous regions flanking NF1 (proximal