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Q37618496-B5152720-F65C-4DB1-9805-384CAFBD977D
Q37618496-B5152720-F65C-4DB1-9805-384CAFBD977D
BestRank
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http://www.wikidata.org/entity/statement/Q37618496-B5152720-F65C-4DB1-9805-384CAFBD977D
Ullrich Congenital Muscular Dystrophy (UCMD): Clinical and Genetic Correlations.
P2860
Q37618496-B5152720-F65C-4DB1-9805-384CAFBD977D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37618496-B5152720-F65C-4DB1-9805-384CAFBD977D
rank
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type
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Statement
wasDerivedFrom
ae9ba84ae0aadd64bdff99e86dd54429ed49072a
P2860
New molecular mechanism for Ullrich congenital muscular dystrophy: a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype.