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Paper Report for: Malki_2020_Genet.Med__

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Title: Loss-of-function variants in C3ORF52 result in localized autosomal recessive hypotrichosis
Malki L, Sarig O, Cesarato N, Mohamad J, Canter T, Assaf S, Pavlovsky M, Vodo D, Anis Y and Sprecher E <9 more author(s)>
Ref: Genet Med, :, 2020 : PubMed

        



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Malki L, Sarig O, Cesarato N, Mohamad J, Canter T, Assaf S, Pavlovsky M, Vodo D, Anis Y, Bihari O, Malovitski K, Gat A, Thiele H, White BEP, Samuelov L, Nanda A, Paller AS, Betz RC, Sprecher E (2020)
Loss-of-function variants in C3ORF52 result in localized autosomal recessive hypotrichosis
Genet Med

Malki L, Sarig O, Cesarato N, Mohamad J, Canter T, Assaf S, Pavlovsky M, Vodo D, Anis Y, Bihari O, Malovitski K, Gat A, Thiele H, White BEP, Samuelov L, Nanda A, Paller AS, Betz RC, Sprecher E (2020)
Genet Med



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