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Q57951762-BCBEF61D-3093-493C-ADDF-45A5FAFDE6A6
Q57951762-BCBEF61D-3093-493C-ADDF-45A5FAFDE6A6
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Statement
http://www.wikidata.org/entity/statement/Q57951762-BCBEF61D-3093-493C-ADDF-45A5FAFDE6A6
Clinical and molecular analysis in families with autosomal recessive osteogenesis imperfecta identifies mutations in five genes and suggests genotype-phenotype correlations
P2860
Q57951762-BCBEF61D-3093-493C-ADDF-45A5FAFDE6A6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q57951762-BCBEF61D-3093-493C-ADDF-45A5FAFDE6A6
rank
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type
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Statement
wasDerivedFrom
2a4b5567e4ec143656edda0284e621191ac7e508
P2860
Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta