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Four New Cases of Hypomyelinating Leukodystrophy Associated with the UFM1 c.-155_-153delTCA Founder Mutation in Pediatric Patients of Roma Descent in Hungary.
Genes (Basel). 2021 Aug 27;12(9):1331. doi: 10.3390/genes12091331.
Genes (Basel). 2021.
PMID: 34573312
Free PMC article.
Report of a Novel ALOX12B Mutation in Self-Improving Collodion Ichthyosis with an Overview of the Genetic Background of the Collodion Baby Phenotype.
Anker P, Kiss N, Kocsis I, Czemmel É, Becker K, Zakariás S, Plázár D, Farkas K, Mayer B, Nagy N, Széll M, Ács N, Szalai Z, Medvecz M.
Anker P, et al. Among authors: czemmel e.
Life (Basel). 2021 Jun 27;11(7):624. doi: 10.3390/life11070624.
Life (Basel). 2021.
PMID: 34199106
Free PMC article.
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