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Q36261015-F59BD7EB-0C48-4AFA-9A7D-A0A21BC5E217
Q36261015-F59BD7EB-0C48-4AFA-9A7D-A0A21BC5E217
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36261015-F59BD7EB-0C48-4AFA-9A7D-A0A21BC5E217
Whole Exome Sequencing Reveals Compound Heterozygosity for Ethnically Distinct PEX7 Mutations Responsible for Rhizomelic Chondrodysplasia Punctata, Type 1.
P1476
Q36261015-F59BD7EB-0C48-4AFA-9A7D-A0A21BC5E217
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36261015-F59BD7EB-0C48-4AFA-9A7D-A0A21BC5E217
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
065a23efbefeb069c8a3b8ef9d3cb02d8b4c79c2
P1476
Whole Exome Sequencing Reveals
......
drodysplasia Punctata, Type 1.
@en