Matches in Nanopublications for { ?s ?p "[We report a novel missense mutation, p.V42M, in CRYGS associated with bilateral congenital cataract in a family of Indian origin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP331818.RAMWB74_6_x82oIgleACi34mn3I2PWE40IpBK2mUY_dEY130_assertion description "[We report a novel missense mutation, p.V42M, in CRYGS associated with bilateral congenital cataract in a family of Indian origin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP331818.RAMWB74_6_x82oIgleACi34mn3I2PWE40IpBK2mUY_dEY130_provenance.
- NP328616.RAo8_8SweM9JyhRmdeN7Wbtt4rJWw9lhXvHJNGjJwHqfA130_assertion description "[We report a novel missense mutation, p.V42M, in CRYGS associated with bilateral congenital cataract in a family of Indian origin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP328616.RAo8_8SweM9JyhRmdeN7Wbtt4rJWw9lhXvHJNGjJwHqfA130_provenance.
- NP723967.RAGo0XU356vqDjpzQcBbi7lLL3B_4-ln43KI2yb4QuFrg130_assertion description "[We report a novel missense mutation, p.V42M, in CRYGS associated with bilateral congenital cataract in a family of Indian origin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723967.RAGo0XU356vqDjpzQcBbi7lLL3B_4-ln43KI2yb4QuFrg130_provenance.