ISIDLB1721 - A novel pathogenic TPCN2 mutation detected for the first time in a Caucasian patient confirms the dominant inheritance of albinism

Széll, Márta; Nagy, Nikoletta; Pál, Margit; Kun, József; Galic, Bence; Medvecz, Márta; Neller, Alexandra; Fábos, Beáta; Danis, Judit; Ádám, Éva; Gyenesei, Attila

doi:10.26226/m.6437c123ed69430011f2f535

2023

DOI: 10.26226/m.6437c123ed69430011f2f535

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ISIDLB1721 - A novel pathogenic TPCN2 mutation detected for the first time in a Caucasian patient confirms the dominant inheritance of albinism

Márta Széll¹,

Nikoletta Nagy²,

Margit Pál³

et al.

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ISIDLB1721 - A novel pathogenic TPCN2 mutation detected for the first time in a Caucasian patient confirms the dominant inheritance of albinism

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