Additional file 1: of Truncating mutation in intracellular phospholipase A1 gene (DDHD2) in hereditary spastic paraplegia with intellectual disability (SPG54)

Alrayes, Nuha; Mohamoud, Hussein; Jelani, Musharraf; Ahmad, Saleem; Vadgama, Nirmal; Bakur, Khadijah; Simpson, Michael; Al-Aama, Jumana; Nasir, Jamal

doi:10.6084/m9.figshare.c.3614948_D1.v1

13104_2015_1227_MOESM1_ESM.docx (15.99 kB)

Additional file 1: of Truncating mutation in intracellular phospholipase A1 gene (DDHD2) in hereditary spastic paraplegia with intellectual disability (SPG54)

journal contribution

posted on 2015-06-27, 05:00 authored by Nuha Alrayes, Hussein Mohamoud, Musharraf Jelani, Saleem Ahmad, Nirmal Vadgama, Khadijah Bakur, Michael Simpson, Jumana Al-Aama, Jamal Nasir

Table S1. List of mutations identified in DDHD2 gene causing hereditary spastic paraplegia (SPG54). Previously reported mutations known to cause the SPG54 phenotype are listed.