| Original Article | ||
JBCGenetics. 2023; 6(1): 22-28 | ||
| 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 03, 2023]. 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 03, 2023]; 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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