M. Umair
发表
A. Wadood,
S. Shams,
Aamir Fahira,
2023,
ACS omega.
Nazish Masud,
M. Alfadhel,
A. Alangari,
2023,
Journal of genetic counseling.
A. Pagnamenta,
L. Hoefsloot,
S. Arold,
2023,
Acta Neuropathologica.
ATP9A deficiency causes ADHD and aberrant endosomal recycling via modulating RAB5 and RAB11 activity
H. Liu,
Huansen Huang,
Haixia Zhuang,
2023,
Molecular Psychiatry.
M. Alfadhel,
Q. Alam,
Mashael Alharbi,
2022,
Molecular genetics & genomic medicine.
A. Shah,
A. Wadood,
P. He,
2022,
Clinical genetics.
I. Iqbal,
S. Shafiq,
Ahmed Waqas,
2022,
Molecular Syndromology.
M. Alfadhel,
S. Shafiq,
M. Younus,
2022,
Frontiers in Genetics.
Chandni Hayat,
Ashraf N. Abdalla,
Junjian Hu,
2023,
Frontiers in Cellular and Infection Microbiology.
S. Arold,
S. Furini,
A. Pinto,
2022,
Frontiers in Molecular Neuroscience.
F. Bibi,
M. Jelani,
Gauhar Rehman,
2023,
The journal of gene medicine.
Muhammad Umair,
M. Umair,
2023,
The journal of gene medicine.
M. Alfadhel,
Q. Alam,
Mashael Alharbi,
2022,
Frontiers in Genetics.
S. Khan,
Q. Alam,
Shazia Khan,
2023,
Genes.
M. Bilal,
O. Palander,
F. Ahmad,
2022,
Clinical genetics.
N. Drouot,
P. Striano,
F. Zara,
2022,
Human mutation.
G. Zaman,
H. Houlden,
Xue Zhang,
2023,
The journal of gene medicine.
K. Shah,
F. Ahmad,
Muhammad Umair,
2023,
Genes.
S. Abbas,
Ahmed Waqas,
M. Aljadani,
2022,
International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience.
Q. Alam,
Zaheer Ahmed,
M. Rafeeq,
2023,
Frontiers in Genetics.
M. Z. Alam,
M. Bilal,
Ahmed Waqas,
2022,
neurogenetics.
A. Rehman,
Ping Li,
Ashraf N. Abdalla,
2023,
Frontiers in Molecular Biosciences.
M. Kakar,
Ahmed Waqas,
M. Rafeeq,
2022,
PloS one.
M. Alfadhel,
F. Al Mutairi,
A. Al Tuwaijri,
2023,
Clinical chemistry.
S. Abbas,
Tayyaba Afsar,
S. Razak,
2023,
Journal of Disability Research.
William E. Byrd,
Gabor T. Marth,
Marni J. Falk,
2023,
American journal of human genetics.