Long-Term Follow-Up of a Case with Dyskeratosis Congenita...

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Acta Haematologica 2019

Long-Term Follow-Up of a Case with Dyskeratosis Congenita Caused by NHP2-V126M/X154R Mutation: Genotype-Phenotype Association

Erdem, Melek, Tüfekçi, Özlem, Yılmaz, Şebnem, Alacacıoğlu, İnci, Ören, Hale
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Year:
2019
Language:
english
Journal:
Acta Haematologica
DOI:
10.1159/000494421
File:
PDF, 306 KB
english, 2019
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