Matches in Nanopublications for { ?s ?p "[The purpose of the present study was to determine the utility and limitations of haplotype-based genetic mapping in estimating the location of the NYX gene, which has recently been identified as the causative gene for a rare inherited retinal disorder known as the complete type of X-linked congenital stationary night blindness (CSNB1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP497208.RAoBvRLbGm9QnBD3EcXLyvgdFwBr1gXOufIYVQxj_zKl8130_assertion description "[The purpose of the present study was to determine the utility and limitations of haplotype-based genetic mapping in estimating the location of the NYX gene, which has recently been identified as the causative gene for a rare inherited retinal disorder known as the complete type of X-linked congenital stationary night blindness (CSNB1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP497208.RAoBvRLbGm9QnBD3EcXLyvgdFwBr1gXOufIYVQxj_zKl8130_provenance.
- NP935889.RAel_6y3FP5PGcXnJQY6aZzCfGKgYIVK0x3z6eIe92MXk130_assertion description "[The purpose of the present study was to determine the utility and limitations of haplotype-based genetic mapping in estimating the location of the NYX gene, which has recently been identified as the causative gene for a rare inherited retinal disorder known as the complete type of X-linked congenital stationary night blindness (CSNB1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP935889.RAel_6y3FP5PGcXnJQY6aZzCfGKgYIVK0x3z6eIe92MXk130_provenance.
- NP935909.RAiaRNRR17Igqr7nQ9UyY7FAqdn0nkHFaIPO8uxAzjrlA130_assertion description "[The purpose of the present study was to determine the utility and limitations of haplotype-based genetic mapping in estimating the location of the NYX gene, which has recently been identified as the causative gene for a rare inherited retinal disorder known as the complete type of X-linked congenital stationary night blindness (CSNB1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP935909.RAiaRNRR17Igqr7nQ9UyY7FAqdn0nkHFaIPO8uxAzjrlA130_provenance.
- NP321067.RAfMw7k1TDY5bzB7VBYRuU-Wg7o7R7ZJ5wtjEg0r4yi68130_assertion description "[The purpose of the present study was to determine the utility and limitations of haplotype-based genetic mapping in estimating the location of the NYX gene, which has recently been identified as the causative gene for a rare inherited retinal disorder known as the complete type of X-linked congenital stationary night blindness (CSNB1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321067.RAfMw7k1TDY5bzB7VBYRuU-Wg7o7R7ZJ5wtjEg0r4yi68130_provenance.
- NP321068.RA-25JggV7cFdgRtScfuysGd2xY1LSYIvSwE3TD9-P8k0130_assertion description "[The purpose of the present study was to determine the utility and limitations of haplotype-based genetic mapping in estimating the location of the NYX gene, which has recently been identified as the causative gene for a rare inherited retinal disorder known as the complete type of X-linked congenital stationary night blindness (CSNB1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321068.RA-25JggV7cFdgRtScfuysGd2xY1LSYIvSwE3TD9-P8k0130_provenance.