Found: 14
Select item for more details and to access through your institution.
The rs1986112 Variant is Associated with Increased RAB8B Gene Expression in Schizophrenic Patients.
- Published in:
- Clinical Laboratory, 2019, v. 65, n. 4, p. 517, doi. 10.7754/Clin.Lab.2018.180832
- By:
- Publication type:
- Article
Expression analysis and genotyping of DGKZ: a GWAS-derived risk gene for schizophrenia.
- Published in:
- Molecular Biology Reports, 2019, v. 46, n. 4, p. 4105, doi. 10.1007/s11033-019-04860-1
- By:
- Publication type:
- Article
Mutational analysis of CYP1B1 gene in Iranian pedigrees with glaucoma reveals known and novel mutations.
- Published in:
- International Ophthalmology, 2021, v. 41, n. 10, p. 3269, doi. 10.1007/s10792-021-01888-w
- By:
- Publication type:
- Article
A novel splice site mutation in the SDCCAG8 gene in an Iranian family with Bardet–Biedl syndrome.
- Published in:
- International Ophthalmology, 2021, v. 41, n. 2, p. 389, doi. 10.1007/s10792-020-01588-x
- By:
- Publication type:
- Article
Bioinformatic tools to determine the pathogenicity of a missense mutation in PKHD1 in autosomal recessive polycystic kidney disease.
- Published in:
- Nephrology, 2017, v. 22, n. 4, p. 330, doi. 10.1111/nep.12919
- By:
- Publication type:
- Article
ANXA1 with Anti-Inflammatory Properties Might Contribute to Parkinsonism.
- Published in:
- 2021
- By:
- Publication type:
- journal article
PRDM12 Is Transcriptionally Active and Required for Nociceptor Function Throughout Life.
- Published in:
- Frontiers in Molecular Neuroscience, 2021, v. 14, p. 1, doi. 10.3389/fnmol.2021.720973
- By:
- Publication type:
- Article
The analysis of association between SNCA, HUSEYO and CSMD1 gene variants and Parkinson's disease in Iranian population.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Clinical and molecular spectrum of P/Q type calcium channel Cav2.1 in epileptic patients.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Erratum to: Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia.
- Published in:
- 2021
- By:
- Publication type:
- journal article
A Novel Ornithine Aminotransferase Splice Site Mutation Causes Vitamin B6-Responsive Gyrate Atrophy.
- Published in:
- Journal of Ophthalmic & Vision Research, 2024, v. 19, n. 1, p. 118, doi. 10.18502/jovr.v19i1.15446
- By:
- Publication type:
- Article
Homozygous Mutation in TWNK Cases Ataxia, Sensorineural Hearing Loss and Optic Nerve Atrophy.
- Published in:
- Archives of Iranian Medicine (AIM), 2019, v. 22, n. 12, p. 728
- By:
- Publication type:
- Article
COL18A1 is a candidate eye iridocorneal angle-closure gene in humans.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 21, p. 3772, doi. 10.1093/hmg/ddy256
- By:
- Publication type:
- Article