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Q33905203-97A257A4-E321-41C5-A5EF-7AF7441C2A90
Q33905203-97A257A4-E321-41C5-A5EF-7AF7441C2A90
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33905203-97A257A4-E321-41C5-A5EF-7AF7441C2A90
New molecular mechanism for Ullrich congenital muscular dystrophy: a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype.
P921
Q33905203-97A257A4-E321-41C5-A5EF-7AF7441C2A90
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33905203-97A257A4-E321-41C5-A5EF-7AF7441C2A90
rank
NormalRank
type
BestRank
Statement
P921
Ullrich congenital muscular dystrophy