Phenotype‐Genotype Correlation in Children with Neurofibromatosis Type 1
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DOI: 10.1055/s-0037-1620239
Abstract: Abstract Neurofibromatosis type 1 (NF1) is a common autosomal dominant disorder with an incidence of ˜1 in 4,000 live births. Neurofibromin, the gene product, is ubiquitously expressed at high levels in the nervous system and… read more here.
Keywords: phenotype genotype; correlation children; genotype correlation; children neurofibromatosis ... See more keywords