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Q34181756-B8C5775C-78F9-457D-98F4-2C2F88DF1A0E
Q34181756-B8C5775C-78F9-457D-98F4-2C2F88DF1A0E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34181756-B8C5775C-78F9-457D-98F4-2C2F88DF1A0E
Molecular defect in siblings with prolidase deficiency and absence or presence of clinical symptoms. A 0.8-kb deletion with breakpoints at the short, direct repeat in the PEPD gene and synthesis of abnormal messenger RNA and inactive polypeptide
P356
Q34181756-B8C5775C-78F9-457D-98F4-2C2F88DF1A0E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34181756-B8C5775C-78F9-457D-98F4-2C2F88DF1A0E
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
928d1cf50ba5ee46cf0ab01b931e2d97f9ab0f09
P356
10.1172/JCI115115
http://www.w3.org/2001/XMLSchema#string
P356
JCI115115