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Q34493831-3E24DFA4-980C-4207-AF33-ED3C5F55AE30
Q34493831-3E24DFA4-980C-4207-AF33-ED3C5F55AE30
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34493831-3E24DFA4-980C-4207-AF33-ED3C5F55AE30
A novel mutation in MIP associated with congenital nuclear cataract in a Chinese family.
P2860
Q34493831-3E24DFA4-980C-4207-AF33-ED3C5F55AE30
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34493831-3E24DFA4-980C-4207-AF33-ED3C5F55AE30
rank
NormalRank
type
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Statement
wasDerivedFrom
d466152189ba133ed0bffdf45c02c28c90d3f086
P2860
Novel single-base deletional mutation in major intrinsic protein (MIP) in autosomal dominant cataract