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Halat P

References (2)

Title : Congenital cochlear deafness in mitochondrial diseases related to RRM2B and SERAC1 gene defects. A study of the mitochondrial patients of the CMHI hospital in Warsaw, Poland - Iwanicka-Pronicka_2019_Int.J.Pediatr.Otorhinolaryngol_121_143
Author(s) : Iwanicka-Pronicka K , Ciara E , Piekutowska-Abramczuk D , Halat P , Pajdowska M , Pronicki M
Ref : Int J Pediatr Otorhinolaryngol , 121 :143 , 2019
Abstract :
PubMedSearch : Iwanicka-Pronicka_2019_Int.J.Pediatr.Otorhinolaryngol_121_143
PubMedID: 30909120
Gene_locus related to this paper: human-SERAC1

Title : New perspective in diagnostics of mitochondrial disorders: two years' experience with whole-exome sequencing at a national paediatric centre - Pronicka_2016_J.Transl.Med_14_174
Author(s) : Pronicka E , Piekutowska-Abramczuk D , Ciara E , Trubicka J , Rokicki D , Karkucinska-Wieckowska A , Pajdowska M , Jurkiewicz E , Halat P , Kosinska J , Pollak A , Rydzanicz M , Stawinski P , Pronicki M , Krajewska-Walasek M , Ploski R
Ref : J Transl Med , 14 :174 , 2016
Abstract :
PubMedSearch : Pronicka_2016_J.Transl.Med_14_174
PubMedID: 27290639
Gene_locus related to this paper: human-SERAC1