Jul 2026
Detection of the NPHP4 c.2999_3005del (p.Asn1000SerfsTer4) variant in an Iranian family with nephronophthisis‐4
Improved understanding of the genetic basis of the disease can provide improved guidance for genetic counseling and family planning strategies for additional affected families, and enhancing the understanding of genotype-phenotype correlations in NPHP4.
Motahareh Jadidi, Shima Booali, Kolsoum Inanloorahatloo
· Zeitschrift für Induktive Ab... · 0 citations