E-ISSN 1658-8088 | ISSN 1658-807X
 

Original Article
Online Published: 23 Mar 2023
 



How to Cite this Article
Pubmed Style

Nayab A, Andleeb S, Zeb S, Manzoor HY, Zehri Z, Mahmood A, Khan H, Umair M, Waqas A. Uncovering the genetic basis of hyperphosphatasia with impaired intellectual development syndrome type 2: identification of a novel biallelic nonsense mutation in PIGO gene. JBCGenetics. 2023; 6(1): 22-28. doi:10.24911/JBCGenetics/183-1673224261


Web Style

Nayab A, Andleeb S, Zeb S, Manzoor HY, Zehri Z, Mahmood A, Khan H, Umair M, Waqas A. Uncovering the genetic basis of hyperphosphatasia with impaired intellectual development syndrome type 2: identification of a novel biallelic nonsense mutation in PIGO gene. https://www.jbcgenetics.com/?mno=137867 [Access: October 10, 2024]. doi:10.24911/JBCGenetics/183-1673224261


AMA (American Medical Association) Style

Nayab A, Andleeb S, Zeb S, Manzoor HY, Zehri Z, Mahmood A, Khan H, Umair M, Waqas A. Uncovering the genetic basis of hyperphosphatasia with impaired intellectual development syndrome type 2: identification of a novel biallelic nonsense mutation in PIGO gene. JBCGenetics. 2023; 6(1): 22-28. doi:10.24911/JBCGenetics/183-1673224261



Vancouver/ICMJE Style

Nayab A, Andleeb S, Zeb S, Manzoor HY, Zehri Z, Mahmood A, Khan H, Umair M, Waqas A. Uncovering the genetic basis of hyperphosphatasia with impaired intellectual development syndrome type 2: identification of a novel biallelic nonsense mutation in PIGO gene. JBCGenetics. (2023), [cited October 10, 2024]; 6(1): 22-28. doi:10.24911/JBCGenetics/183-1673224261



Harvard Style

Nayab, A., Andleeb, . S., Zeb, . S., Manzoor, . H. Y., Zehri, . Z., Mahmood, . A., Khan, . H., Umair, . M. & Waqas, . A. (2023) Uncovering the genetic basis of hyperphosphatasia with impaired intellectual development syndrome type 2: identification of a novel biallelic nonsense mutation in PIGO gene. JBCGenetics, 6 (1), 22-28. doi:10.24911/JBCGenetics/183-1673224261



Turabian Style

Nayab, Anam, Shagufta Andleeb, Shah Zeb, Hafiza Yasmin Manzoor, Zamrud Zehri, Arif Mahmood, Hammal Khan, Muhammad Umair, and Ahmed Waqas. 2023. Uncovering the genetic basis of hyperphosphatasia with impaired intellectual development syndrome type 2: identification of a novel biallelic nonsense mutation in PIGO gene. Journal of Biochemical and Clinical Genetics, 6 (1), 22-28. doi:10.24911/JBCGenetics/183-1673224261



Chicago Style

Nayab, Anam, Shagufta Andleeb, Shah Zeb, Hafiza Yasmin Manzoor, Zamrud Zehri, Arif Mahmood, Hammal Khan, Muhammad Umair, and Ahmed Waqas. "Uncovering the genetic basis of hyperphosphatasia with impaired intellectual development syndrome type 2: identification of a novel biallelic nonsense mutation in PIGO gene." Journal of Biochemical and Clinical Genetics 6 (2023), 22-28. doi:10.24911/JBCGenetics/183-1673224261



MLA (The Modern Language Association) Style

Nayab, Anam, Shagufta Andleeb, Shah Zeb, Hafiza Yasmin Manzoor, Zamrud Zehri, Arif Mahmood, Hammal Khan, Muhammad Umair, and Ahmed Waqas. "Uncovering the genetic basis of hyperphosphatasia with impaired intellectual development syndrome type 2: identification of a novel biallelic nonsense mutation in PIGO gene." Journal of Biochemical and Clinical Genetics 6.1 (2023), 22-28. Print. doi:10.24911/JBCGenetics/183-1673224261



APA (American Psychological Association) Style

Nayab, A., Andleeb, . S., Zeb, . S., Manzoor, . H. Y., Zehri, . Z., Mahmood, . A., Khan, . H., Umair, . M. & Waqas, . A. (2023) Uncovering the genetic basis of hyperphosphatasia with impaired intellectual development syndrome type 2: identification of a novel biallelic nonsense mutation in PIGO gene. Journal of Biochemical and Clinical Genetics, 6 (1), 22-28. doi:10.24911/JBCGenetics/183-1673224261





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