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2
Q35361558-74D7249B-0D0A-4880-8374-E089414440FA
Q35361558-74D7249B-0D0A-4880-8374-E089414440FA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35361558-74D7249B-0D0A-4880-8374-E089414440FA
Mutations in SPECC1L, encoding sperm antigen with calponin homology and coiled-coil domains 1-like, are found in some cases of autosomal dominant Opitz G/BBB syndrome
P1476
Q35361558-74D7249B-0D0A-4880-8374-E089414440FA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35361558-74D7249B-0D0A-4880-8374-E089414440FA
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
ffbec7288ebe5c6c4b724646feb8429b2cd96ab9
P1476
Mutations in SPECC1L, encoding
......
dominant Opitz G/BBB syndrome
@en