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Q53091941-39709521-CB0D-4BA7-B0E6-171C6984086A
Q53091941-39709521-CB0D-4BA7-B0E6-171C6984086A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q53091941-39709521-CB0D-4BA7-B0E6-171C6984086A
Expanding the mutation spectrum in 130 probands with ARPKD: identification of 62 novel PKHD1 mutations by sanger sequencing and MLPA analysis.
P2860
Q53091941-39709521-CB0D-4BA7-B0E6-171C6984086A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q53091941-39709521-CB0D-4BA7-B0E6-171C6984086A
rank
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type
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Statement
wasDerivedFrom
6ae5254fb03c4646efe732b885d178581f23e44f
P2860
Multi-exon deletions of the PKHD1 gene cause autosomal recessive polycystic kidney disease (ARPKD).