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Q57987662-21253451-D099-491E-824F-77D9B6FDDF9E
Q57987662-21253451-D099-491E-824F-77D9B6FDDF9E
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Statement
http://www.wikidata.org/entity/statement/Q57987662-21253451-D099-491E-824F-77D9B6FDDF9E
Genetic cause and prevalence of hydroxyprolinemia
P2860
Q57987662-21253451-D099-491E-824F-77D9B6FDDF9E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q57987662-21253451-D099-491E-824F-77D9B6FDDF9E
rank
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wasDerivedFrom
3bf588602e6dc7ca8818095d3b8d03873d18344e
P2860
Phenotypic spectrum of eleven patients and five novel MTFMT mutations identified by exome sequencing and candidate gene screening.