Matches in Nanopublications for { ?s ?p "[Griscelli syndrome type 2 is a rare autosomal recessive primary immunodeficiency disease caused by a mutation in the RAB27A gene and characterized by oculocutaneous hypopigmentation and variable cellular immunodeficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP265414.RAfxxboadNBOdqixbNshy0oQW-uqVCwKmHozrsCe9bDZ0130_assertion description "[Griscelli syndrome type 2 is a rare autosomal recessive primary immunodeficiency disease caused by a mutation in the RAB27A gene and characterized by oculocutaneous hypopigmentation and variable cellular immunodeficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP265414.RAfxxboadNBOdqixbNshy0oQW-uqVCwKmHozrsCe9bDZ0130_provenance.
- NP645951.RAr067QXi9o0uDTdSnsS8hl1QxHlQ5JMYETUG0X3IvqvM130_assertion description "[Griscelli syndrome type 2 is a rare autosomal recessive primary immunodeficiency disease caused by a mutation in the RAB27A gene and characterized by oculocutaneous hypopigmentation and variable cellular immunodeficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP645951.RAr067QXi9o0uDTdSnsS8hl1QxHlQ5JMYETUG0X3IvqvM130_provenance.
- NP663768.RAZJJgWn-R-9YWs1MJzM0QoWoRI63NrRJ1iwGlkHY5rZg130_assertion description "[Griscelli syndrome type 2 is a rare autosomal recessive primary immunodeficiency disease caused by a mutation in the RAB27A gene and characterized by oculocutaneous hypopigmentation and variable cellular immunodeficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP663768.RAZJJgWn-R-9YWs1MJzM0QoWoRI63NrRJ1iwGlkHY5rZg130_provenance.
- NP601969.RAWvLLraOIMiZgBmeYO0P8n0nItVIb9yN7_W6B5-KzjIM130_assertion description "[Griscelli syndrome type 2 is a rare autosomal recessive primary immunodeficiency disease caused by a mutation in the RAB27A gene and characterized by oculocutaneous hypopigmentation and variable cellular immunodeficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP601969.RAWvLLraOIMiZgBmeYO0P8n0nItVIb9yN7_W6B5-KzjIM130_provenance.
- NP662876.RAU5Cgz07sPDDTTvqsqngVsp0hC39HiHdGnsY89fhr7Xs130_assertion description "[Griscelli syndrome type 2 is a rare autosomal recessive primary immunodeficiency disease caused by a mutation in the RAB27A gene and characterized by oculocutaneous hypopigmentation and variable cellular immunodeficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662876.RAU5Cgz07sPDDTTvqsqngVsp0hC39HiHdGnsY89fhr7Xs130_provenance.
- assertion description "[Griscelli syndrome type 2 is a rare autosomal recessive primary immunodeficiency disease caused by a mutation in the RAB27A gene and characterized by oculocutaneous hypopigmentation and variable cellular immunodeficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP871754.RAbtIVIf7AHlm403iRt8GqqB1Jr-XojX6Z8fwW6sydLLw130_assertion description "[Griscelli syndrome type 2 is a rare autosomal recessive primary immunodeficiency disease caused by a mutation in the RAB27A gene and characterized by oculocutaneous hypopigmentation and variable cellular immunodeficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP871754.RAbtIVIf7AHlm403iRt8GqqB1Jr-XojX6Z8fwW6sydLLw130_provenance.
- NP662850.RAiPr5U3K5QaEcDvQXqgjRHPJE6hEx2rtuTQ9U7jI_6Ts130_assertion description "[Griscelli syndrome type 2 is a rare autosomal recessive primary immunodeficiency disease caused by a mutation in the RAB27A gene and characterized by oculocutaneous hypopigmentation and variable cellular immunodeficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662850.RAiPr5U3K5QaEcDvQXqgjRHPJE6hEx2rtuTQ9U7jI_6Ts130_provenance.
- NP662854.RAjRr_t1EkuTGHN5-rpZA8-9Th67bA0boWCBG0S3KLLGU130_assertion description "[Griscelli syndrome type 2 is a rare autosomal recessive primary immunodeficiency disease caused by a mutation in the RAB27A gene and characterized by oculocutaneous hypopigmentation and variable cellular immunodeficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662854.RAjRr_t1EkuTGHN5-rpZA8-9Th67bA0boWCBG0S3KLLGU130_provenance.
- NP871755.RAlXW5vR_N0Wc5A-nb2oz8IS3hpGBSzqBQf1-iN9BWSwU130_assertion description "[Griscelli syndrome type 2 is a rare autosomal recessive primary immunodeficiency disease caused by a mutation in the RAB27A gene and characterized by oculocutaneous hypopigmentation and variable cellular immunodeficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP871755.RAlXW5vR_N0Wc5A-nb2oz8IS3hpGBSzqBQf1-iN9BWSwU130_provenance.
- NP871753.RA6UD3HqlYh-zFL8lszmPZLb1LzQ6HRXT78NjrFaTHd4k130_assertion description "[Griscelli syndrome type 2 is a rare autosomal recessive primary immunodeficiency disease caused by a mutation in the RAB27A gene and characterized by oculocutaneous hypopigmentation and variable cellular immunodeficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP871753.RA6UD3HqlYh-zFL8lszmPZLb1LzQ6HRXT78NjrFaTHd4k130_provenance.