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Q34320437-C07CC7C0-419E-4419-9F41-C5B0169D5B98
Q34320437-C07CC7C0-419E-4419-9F41-C5B0169D5B98
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http://www.wikidata.org/entity/statement/Q34320437-C07CC7C0-419E-4419-9F41-C5B0169D5B98
SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity.
P2860
Q34320437-C07CC7C0-419E-4419-9F41-C5B0169D5B98
BestRank
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http://www.wikidata.org/entity/statement/Q34320437-C07CC7C0-419E-4419-9F41-C5B0169D5B98
rank
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wasDerivedFrom
05fadbd80cb40a09775de54a37576eb04c1d24a9
P2860
Insights into the PX (phox-homology) domain and SNX (sorting nexin) protein families: structures, functions and roles in disease.