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Possible modifier genes in the variation of neurofibromatosis type 1 clinical phenotypes 

Sharafi, Parisa; Ayter, Şükriye (Taylor and Francis Ltd, 2018-04-03)
Neurofibromatosis type 1 (NF1) is the most common neurogenetic disorder worldwide, caused by mutations in the (NF1) gene. Although NF1 is a single-gene disorder with autosomal-dominant inheritance, its clinical expression ...

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AuthorAyter, Şükriye (1)Sharafi, Parisa (1)SubjectClinical variability (1)
Genotype–phenotype correlation (1)
Modifier genes (1)Neurofibromatosis type 1 (1)... View MoreDate Issued2018 (1)Has File(s)Yes (1)Typearticle (1)CoverageMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı (1)WOSWOS:000434269300002 (1)Scopus2-s2.0-85048232895 (1)Dileng (1)Erişiminfo:eu-repo/semantics/openAccess (1)

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