Biología Celular, Genética, Histología y Farmacología
Saila
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Children's Hospital of Philadelphia
Filadelfia, Estados UnidosChildren's Hospital of Philadelphia-ko ikertzaileekin lankidetzan egindako argitalpenak (1)
2020
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Exome sequencing identifies PEX6 mutations in three cases diagnosed with Retinitis Pigmentosa and hearing impairment
Molecular Vision, Vol. 26, pp. 216-225