Clinical characterisation of 29 neurofibromatosis type-1 patients with molecularly ascertained 1.4 Mb type-1 NF1 deletions.
Beteiligte Einrichtungen
Abstract
Large deletions of the NF1 gene region occur in approximately 5% of patients with neurofibromatosis type-1 (NF1) and are associated with particularly severe manifestations of the disease. However, until now, the genotype-phenotype relationship has not been comprehensively studied in patients harbouring large NF1 gene deletions of comparable extent (giving rise to haploinsufficiency of the same genes).
Bibliografische Daten
| Originalsprache | Deutsch |
|---|---|
| Aufsatznummer | 9 |
| ISSN | 0022-2593 |
| Status | Veröffentlicht - 2010 |
| pubmed | 20543202 |
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