Mutational landscape of TRPC6, WT1, LMX1B, APOL1, PTPRO, PMM2, LAMB2 and WT1 genes associated with Steroid resistant nephrotic syndrome.

Thakor, Jinal M; Parmar, Glory; Mistry, Kinnari N; Gang, Sishir; Rank, Dharamshibhai N; Joshi, Chaitanya G

Thakor, Jinal M; Parmar, Glory; Mistry, Kinnari N; Gang, Sishir; Rank, Dharamshibhai N; Joshi, Chaitanya G.

Afiliación

Thakor JM; Ashok and Rita Patel Institute of Integrated Study and Research in Biotechnology and Allied Sciences, ADIT Campus, New Vallabh Vidyanagar, 388121, Anand, Gujarat, India.
Parmar G; Ashok and Rita Patel Institute of Integrated Study and Research in Biotechnology and Allied Sciences, ADIT Campus, New Vallabh Vidyanagar, 388121, Anand, Gujarat, India.
Mistry KN; Ashok and Rita Patel Institute of Integrated Study and Research in Biotechnology and Allied Sciences, ADIT Campus, New Vallabh Vidyanagar, 388121, Anand, Gujarat, India. kinnarimistry@aribas.edu.in.
Gang S; Muljibhai Patel Urological Hospital, Dr. V.V. Desai Road, Nadiad, 387001, Gujarat, India.
Rank DN; Department of Animal Breeding and Genetics, College of Veterinary Sciences and Animal Husbandry, Anand Agricultural University, Anand, 388110, Gujarat, India.
Joshi CG; Department of Animal Biotechnology, College of Veterinary Sciences and Animal Husbandry, Anand Agricultural University, Anand, 388110, Gujarat, India.

Mol Biol Rep ; 48(11): 7193-7201, 2021 Nov.

Article en En | MEDLINE | ID: mdl-34546508

Asunto(s)

Predisposición Genética a la Enfermedad; Mutación; Síndrome Nefrótico/genética; Niño; Preescolar; Análisis Mutacional de ADN; Femenino; Genes del Tumor de Wilms; Humanos; Proteínas con Homeodominio LIM/genética; Laminina/genética; Masculino; Fosfotransferasas (Fosfomutasas)/genética; Proteínas Tirosina Fosfatasas Clase 3 Similares a Receptores/genética; Canal Catiónico TRPC6/genética; Factores de Transcripción/genética

Palabras clave

Illumina panel sequencing; Indian patients; Steroid resistant nephrotic syndrome (SRNS); Steroid sensitive nephrotic syndrome (SSNS)

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Mutación / Síndrome Nefrótico Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Mol Biol Rep Año: 2021 Tipo del documento: Article País de afiliación: India Pais de publicación: Países Bajos

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