Semantic Scholar Open Access 2021 2 sitasi

Mutation Analysis of a Pakistani Oculocutaneous Albinism Family Identifies a Novel Splice Site Defect in OCA2 Gene

H. Gul

Lihat Sumber DOI

Abstrak

1Department of Biological Sciences, Faculty of Sciences, Gomal University, D.I. Khan, 29050, Pakistan. 2Molecular Neuropsychiatry and Development Lab (MiND), Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, University of Toronto, ON, Canada. 3Gomal Centre of Biochemistry and Biotechnology, Gomal University, D.I. Khan, Pakistan. 4Department of Psychiatry, University of Toronto, Canada. Article Information Received 01 May 2020 Revised 30 July 2020 Accepted 17 October 2020 Available online 09 June 2021

Topik & Kata Kunci

Biology

Penulis (1)

H. Gul

Format Sitasi

APA MLA BibTeX

Gul, H. (2021). Mutation Analysis of a Pakistani Oculocutaneous Albinism Family Identifies a Novel Splice Site Defect in OCA2 Gene. https://doi.org/10.17582/JOURNAL.PJZ/20200501060515

Akses Cepat

Lihat di Sumber doi.org/10.17582/JOURNAL.PJZ/20200501060515

Informasi Jurnal

Tahun Terbit: 2021
Bahasa: en
Total Sitasi: 2×
Sumber Database: Semantic Scholar
DOI: 10.17582/JOURNAL.PJZ/20200501060515
Akses: Open Access ✓