Primary hyperoxaluria: Comprehensive mutation screening of the disease causing genes and spectrum of disease‐associated pathogenic variants-Reference-Cited by-同舟云学术

Primary hyperoxaluria: Comprehensive mutation screening of the disease causing genes and spectrum of disease‐associated pathogenic variants

Published:2022-10-09 Issue:1 Volume:103 Page:53-66
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clinical Genetics

Author:

Abid Aiysha¹^ORCID,Raza Ali¹,Khan Abdul Rafay¹,Firasat Sadaf¹,Shahid Saba²,Hashmi Seema³,Zafar Mirza Naqi⁴,Sultan Sajid⁵,Khaliq Shagufta⁶,Rizvi Syed Adib‐ul‐Hasan⁷

Affiliation:

1. Centre for Human Genetics and Molecular Medicine Sindh Institute of Urology and Transplantation Karachi Pakistan

2. Molecular Diagnostic Laboratory Al Qassimi Hospital Sharjah UAE

3. Department of Pediatric Nephrology Sindh Institute of Urology and Transplantation Karachi Pakistan

4. Department of Pathology Sindh Institute of Urology and Transplantation Karachi Pakistan

5. Department of Pediatric Urology Sindh Institute of Urology and Transplantation Karachi Pakistan

6. Department of Human Genetics & Molecular Biology University of Health Sciences Lahore Pakistan

7. Department of Urology Sindh Institute of Urology and Transplantation Karachi Pakistan

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.14240

Reference44 articles.

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2. Primary Hyperoxaluria

3. Characteristics and Outcomes of Children with Primary Oxalosis Requiring Renal Replacement Therapy

4. End-stage renal disease in Kuwaiti children: An 8-year experience

5. End-stage renal disease of the Tunisian child: epidemiology, etiologies, and outcome

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