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Q33706467-54ADE16B-E2E6-4C6C-949F-596449AE891D
Q33706467-54ADE16B-E2E6-4C6C-949F-596449AE891D
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Statement
http://www.wikidata.org/entity/statement/Q33706467-54ADE16B-E2E6-4C6C-949F-596449AE891D
Next-generation sequencing for D47N mutation in Cx50 analysis associated with autosomal dominant congenital cataract in a six-generation Chinese family.
P2860
Q33706467-54ADE16B-E2E6-4C6C-949F-596449AE891D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33706467-54ADE16B-E2E6-4C6C-949F-596449AE891D
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Statement
wasDerivedFrom
06e535e68744391f66c7e3d363e7f9a54571925b
P2860
A novel connexin 50 gene (gap junction protein, alpha 8) mutation associated with congenital nuclear and zonular pulverulent cataract.