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Q35602775-235EBC59-99BC-400C-9101-ECC62013ACEC
Q35602775-235EBC59-99BC-400C-9101-ECC62013ACEC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35602775-235EBC59-99BC-400C-9101-ECC62013ACEC
Dominant De Novo Mutations in GJA1 Cause Erythrokeratodermia Variabilis et Progressiva, without Features of Oculodentodigital Dysplasia.
P2860
Q35602775-235EBC59-99BC-400C-9101-ECC62013ACEC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35602775-235EBC59-99BC-400C-9101-ECC62013ACEC
rank
NormalRank
type
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Statement
wasDerivedFrom
f73535de88ffffe36a6a46a197654422eb16d52e
P2860
A nonsense mutation in the first transmembrane domain of connexin 43 underlies autosomal recessive oculodentodigital syndrome