The c.1138G>A Variant of Fibroblast Growth Factor Receptor 3 is a Common Cause of Achondroplasia in Pakistan

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The c.1138G>A Variant of Fibroblast Growth Factor Receptor 3 is a Common Cause of Achondroplasia in Pakistan

Niaz Muhammad¹, Samina Yasin¹, Zunaira Fatima¹, Noor ul Ain¹,

Muhammad Faizan² and Sadaf Naz¹*

Author Affiliations

¹School of Biological Sciences, University of the Punjab, Quaid-e-Azam Campus, Lahore

²Institute of Process Engineering, University of the Chinese Academy of Sciences, Beijing 100190, China

Niaz Muhammad and Samina Yasinshould be considered joint first author.

* Corresponding author: [email protected]

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Fig. 1.

(a) Pedigree of the family ACH8 in which members exhibited dominantly inherited achondroplasia. (b) Chromatogram for FGFR3 selected region showing the most common transition c.G1138>A variant. The arrow indicates the point of mutation.

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December 2021

Vol. 53, Iss. 6, Pages 2001-2521

Pakistan Journal of Zoology

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The c.1138G>A Variant of Fibroblast Growth Factor Receptor 3 is a Common Cause of Achondroplasia in Pakistan

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The c.1138G>A Variant of Fibroblast Growth Factor Receptor 3 is a Common Cause of Achondroplasia in Pakistan

Niaz Muhammad¹, Samina Yasin¹, Zunaira Fatima¹, Noor ul Ain¹,

Muhammad Faizan² and Sadaf Naz¹*

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The c.1138G>A Variant of Fibroblast Growth Factor Receptor 3 is a Common Cause of Achondroplasia in Pakistan

The c.1138G>A Variant of Fibroblast Growth Factor Receptor 3 is a Common Cause of Achondroplasia in Pakistan

Niaz Muhammad1, Samina Yasin1, Zunaira Fatima1, Noor ul Ain1, Muhammad Faizan2 and Sadaf Naz1*

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Niaz Muhammad¹, Samina Yasin¹, Zunaira Fatima¹, Noor ul Ain¹,

Muhammad Faizan² and Sadaf Naz¹*