Mutation Spectrum and Genotype–Phenotype Analyses in a Pakistani Cohort With Hemophilia B

This study aimed to (1) identify F9 genetic alterations in patients with hemophilia B (HB) of Pakistani origin and (2) determine the genotype–phenotype relationships in these patients. Diagnosed cases of HB were identified through registries at designated tertiary health-care centers across the coun...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Clin Appl Thromb Hemost
Prif Awduron: Khan, Muhammad Tariq Masood, Naz, Arshi, Ahmed, Jawad, Shamsi, Tahir, Ahmed, Shariq, Ahmed, Nisar, Imran, Ayisha, Farooq, Nazish, Khan, Muhammad Tariq Hamayun, Taj, Abid Sohail
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: SAGE Publications 2017
Pynciau:
Original Articles
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC6714882/
https://ncbi.nlm.nih.gov/pubmed/28752769
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1076029617721011
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