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Cited by in F6Publishing
For: Bahena P, Daftarian N, Maroofian R, Linares P, Villalobos D, Mirrahimi M, Rad A, Doll J, Hofrichter MAH, Koparir A, Röder T, Han S, Sabbaghi H, Ahmadieh H, Behboudi H, Villanueva-Mendoza C, Cortés-Gonzalez V, Zamora-Ortiz R, Kohl S, Kuehlewein L, Darvish H, Alehabib E, Arenas-Sordo ML, Suri F, Vona B, Haaf T. Unraveling the genetic complexities of combined retinal dystrophy and hearing impairment. Hum Genet 2021. [PMID: 34148116 DOI: 10.1007/s00439-021-02303-1] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
Number Citing Articles
1 Manyisa N, Schrauwen I, de Souza Rios LA, Mowla S, Tekendo-Ngongang C, Popel K, Esoh K, Bharadwaj T, Nouel-Saied LM, Acharya A, Nasir A, Wonkam-Tingang E, Kock C, Dandara C, Leal SM, Wonkam A. A Monoallelic Variant in REST Is Associated with Non-Syndromic Autosomal Dominant Hearing Impairment in a South African Family. Genes (Basel) 2021;12:1765. [PMID: 34828371 DOI: 10.3390/genes12111765] [Reference Citation Analysis]
2 Acharya A, Schrauwen I, Leal SM. Identification of autosomal recessive nonsyndromic hearing impairment genes through the study of consanguineous and non-consanguineous families: past, present, and future. Hum Genet 2021. [PMID: 34291353 DOI: 10.1007/s00439-021-02309-9] [Reference Citation Analysis]