WT1 mutations in patients with Denys-Drash syndrome: a novel mutation in exon 8 and paternal allele origin
Year: 1994
Type: article
Study design: Case Report
Source: Human Genetics
DOI: 10.1007/bf00210593
Institutions: Karolinska University Hospital, Karolinska Institutet
Language: English
Topic: Renal and related cancers
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2081584565