Published June 9, 2023 | Version v1
Dataset Restricted

dataset related to submitted article "Novel HSPG2 gene mutation causing Schwartz-Jampel syndrome in a Moroccan family and review of the literature"

Authors/Creators

  • 1. Fondazione IRCCS Istituto Neurologico Carlo Besta

Description

Next Generation Sequencing, real-time, sequensing cDNA

Notes

This work was supported by the Italian Ministry of Health (RRC_2023).

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