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Clinical and genetic features of four patients with Pearson syndrome: An observational study

Pearson syndrome (PS) is a multisystem mitochondrial cytopathy arising from deletions in mitochondrial DNA. Pearson syndrome is a sporadic disease that affects the hematopoietic system, pancreas, eyes, liver, and heart and the prognosis is poor. Causes of morbidity include metabolic crisis, bone mar...

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Detalles Bibliográficos
Autores principales:	Son, Ji Soo, Seo, Go Hun, Kim, Yoon-Myung, Kim, Gu-Hwan, Jin, Hee Kyung, Bae, Jae-sung, Im, Ho Joon, Yoo, Han-Wook, Lee, Beom Hee
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Lippincott Williams & Wilkins 2022
Materias:	3500
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8812667/ https://www.ncbi.nlm.nih.gov/pubmed/35119049 http://dx.doi.org/10.1097/MD.0000000000028793

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