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The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophy.
- Published in:
- Orphanet Journal of Rare Diseases, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1172-8-16
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- Publication type:
- Article
The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophy.
- Published in:
- 2013
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- Publication type:
- journal article
Computational Analysis of Single Nucleotide Polymorphisms Associated with Altered Drug Responsiveness in Type 2 Diabetes.
- Published in:
- International Journal of Molecular Sciences, 2016, v. 17, n. 7, p. 1008, doi. 10.3390/ijms17071008
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- Publication type:
- Article
Molecular Diagnosis of Usher Syndrome: Application of Two Different Next Generation Sequencing-Based Procedures.
- Published in:
- PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0043799
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- Publication type:
- Article
Identification and characterisation of the retinitis pigmentosa 1-like1 gene (RP1L1): a novel candidate for retinal degenerations.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 2, p. 155, doi. 10.1038/sj.ejhg.5200942
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- Publication type:
- Article
Pharmacogenomics of Drug Response in Type 2 Diabetes: Toward the Definition of Tailored Therapies?
- Published in:
- PPAR Research, 2015, v. 2015, p. 1, doi. 10.1155/2015/415149
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- Publication type:
- Article
Gene Therapy for Leber's Congenital Amaurosis is Safe and Effective Through 1.5 Years After Vector Administration.
- Published in:
- Molecular Therapy, 2010, v. 18, n. 3, p. 643, doi. 10.1038/mt.2009.277
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- Publication type:
- Article