Case report: Disease phenotype associated with simultaneous biallelic mutations in ABCA4 and USH2A due to uniparental disomy of chromosome 1
Villafuerte-De la Cruz, R., Chacon-Camacho, O. F., Rodriguez-Martinez, A. C., Xilotl-De Jesus, N., Arce-Gonzalez, R., Rodriguez-De la Torre, C., Valdez-Garcia, J. E., Rojas-Martinez, A., Zenteno, J. C.
Published in Frontiers in genetics (16.08.2022)
Published in Frontiers in genetics (16.08.2022)
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Journal Article
Case report: Disease phenotype associated with simultaneous biallelic mutations in ABCA4 and USH2A due to uniparental disomy of chromosome 1
Villafuerte-De la Cruz, R, Chacon-Camacho, O F, Rodriguez-Martinez, A C, Xilotl-De Jesus, N, Arce-Gonzalez, R, Rodriguez-De la Torre, C, Valdez-Garcia, J E, Rojas-Martinez, A, Zenteno, J C
Published in Frontiers in genetics (01.01.2022)
Published in Frontiers in genetics (01.01.2022)
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