Publications by authors named "Saima Mustafa"

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An application of fuzzy bipolar weighted correlation coefficient in decision-making problem.
Saima Mustafa, Sadia Mahmood, Zabidin Salleh

PLoS One· December 2023

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A Missense Mutation (c.1037 G > C, p. R346P) in Gene Results in Autosomal Recessive form of Brachyolmia Type 1 (Hobaek Form) in A Consanguineous Family.
Saima Mustafa, Malik Fiaz Hussain, Muhammad Latif, Maryam Ijaz, Muhammad Asif

Genes (Basel)· November 2022

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A novel homozygous missense variant in MATN3 causes spondylo-epimetaphyseal dysplasia Matrilin 3 type in a consanguineous family.
Samina Yasin, Saima Mustafa, Arzoo Ayesha, Muhammad Latif, Mubashir Hassan

Eur J Med Genet· August 2020

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A novel nonsense mutation in NPR2 gene causing Acromesomelic dysplasia, type Maroteaux in a consanguineous family in Southern Punjab (Pakistan).
Saima Mustafa, Zafrin Akhtar, Muhammad Latif, Mubashir Hassan, Muhammad Faisal

Genes Genomics· August 2020

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Analytical Solutions of Fractional-Order Diffusion Equations by Natural Transform Decomposition Method.
Rasool Shah, Hassan Khan, Saima Mustafa, Poom Kumam, Muhammad Arif

Entropy (Basel)· June 2019

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Association of Single Nucleotide Polymorphisms in XRCC1 (194) and XPD (751) with Age-related cataract.
Tafheem Khosa, Sana Aslam, Saima Mustafa, Atif Akbar, Rehan Sadiq Shaikh

Int Ophthalmol· June 2018

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A missense point mutation in COL10A1 identified with whole-genome deep sequencing in a 7-generation Pakistan dwarf family.
Chao Zhang, Jiaojiao Liu, Furhan Iqbal, Yan Lu, Saima Mustafa

Heredity (Edinb)· January 2018

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Association of single nucleotide polymorphism in CD28(C/T-I3 + 17) and CD40 (C/T-1) genes with the Graves' disease.
Saima Mustafa, Hira Fatima, Sadia Fatima, Tafheem Khosa, Atif Akbar

J Pak Med Assoc· January 2018

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