Identification of a Novel Nonsense Mutation in SH2D1A in a Patient With X-Linked Lymphoproliferative Syndrome Type 1: A Case Report
BMC Medical Genetics - United Kingdom
doi 10.1186/s12881-018-0576-y
Full Text
Open PDFAbstract
Available in full text
Categories
Date
April 12, 2018
Authors
Publisher
Springer Science and Business Media LLC