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Q38986089-A66D7D61-7B9E-43AE-9155-5B7A11D86F1C
Q38986089-A66D7D61-7B9E-43AE-9155-5B7A11D86F1C
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http://www.wikidata.org/entity/statement/Q38986089-A66D7D61-7B9E-43AE-9155-5B7A11D86F1C
Corneal dystrophy-causing SLC4A11 mutants: suitability for folding-correction therapy.
P2860
Q38986089-A66D7D61-7B9E-43AE-9155-5B7A11D86F1C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38986089-A66D7D61-7B9E-43AE-9155-5B7A11D86F1C
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wasDerivedFrom
0c48cd070faa27f430ff5bba968ef6310c9b02b6
P2860
Novel SLC4A11 mutations in patients with recessive congenital hereditary endothelial dystrophy (CHED2). Mutation in brief #958. Online.