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UnknownIdentification of 2 novel homozygous mutations in the methylmalonyl-CoA mutase gene in Saudi patients.
Not available
S-EPMC4613637 | biostudies-literature
UnknownA novel mutation in ornithine transcarbamylase gene causing mild intermittent hyperammonemia.
Not available
S-EPMC4621731 | biostudies-literature
UnknownAbsence of mtDNA mutations in leukocytes of CADASIL patients.
Not available
S-EPMC2518270 | biostudies-literature
TranscriptomicsGenomewide methylation analysis in Silver Russell syndrome patients
Genomewide methylation analysis in Silver Russell syndrome patients compared to healthy controls Bisulphite converted DNA from the 24 samples were hybridised to the Illumina Infinium 450k Human Methylation Beadchip
ORGANISM(S): Homo sapiens 
2015-01-12 | E-GEOD-55491 | biostudies-arrayexpress
UnknownAnalysis of the VSX1 gene in keratoconus patients from Saudi Arabia.
Not available
S-EPMC3056127 | biostudies-literature
UnknownA microdeletion in the GRHL2 Gene in two unrelated patients with congenital fibrosis of the extra ocular muscles.
Not available
S-EPMC5674732 | biostudies-literature
UnknownEurasian and Sub-Saharan African mitochondrial DNA haplogroup influences pseudoexfoliation glaucoma development in Saudi patients.
Not available
S-EPMC3044700 | biostudies-literature
UnknownScreening of the Seed Region of MIR184 in Keratoconus Patients from Saudi Arabia.
Not available
S-EPMC4561303 | biostudies-literature
UnknownA new biological and clinical resource for research into pregnancy complications: The Baby Bio Bank.
Not available
S-EPMC5062948 | biostudies-literature
UnknownCase-control association between CCT-associated variants and keratoconus in a Saudi Arabian population.
Not available
S-EPMC4461978 | biostudies-literature
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