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1
Q36095344-3BAC9718-38A1-498D-B99F-9A85A47B6227
Q36095344-3BAC9718-38A1-498D-B99F-9A85A47B6227
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36095344-3BAC9718-38A1-498D-B99F-9A85A47B6227
An atypical case of familial glucocorticoid deficiency without pigmentation caused by coexistent homozygous mutations in MC2R (T152K) and MC1R (R160W).
P50
Q36095344-3BAC9718-38A1-498D-B99F-9A85A47B6227
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36095344-3BAC9718-38A1-498D-B99F-9A85A47B6227
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
4a965ca6aa3eb3b78af0e7c077f9700c265eb0d1
P1545
1
http://www.w3.org/2001/XMLSchema#string
P50
Serap Turan