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Ngu, Lock Hock
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1

Corrigendum to: Prevalence of DDC genotypes in patients wit..:

Himmelreich, Nastassja ; Bertoldi, Mariarita ; Alfadhel, Majid...
Molecular Genetics and Metabolism.  139 (2023)  4 - p. 107647 , 2023
Link: https://doi.org/10.1016/..
 
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2

Prevalence of DDC genotypes in patients with aromatic L-ami..:

Himmelreich, Nastassja ; Bertoldi, Mariarita ; Alfadhel, Majid...
Molecular Genetics and Metabolism.  139 (2023)  3 - p. 107624 , 2023
Link: https://doi.org/10.1016/..
 
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3

Myoclonus‐Ataxia Syndrome Associated with Hyperprolinemia T..:

Ong, Tien Lee ; Lau, Yue Hui ; Ngu, Lock Hock...
Movement Disorders Clinical Practice.  10 (2023)  S3 - p. , 2023
Link: https://doi.org/10.1002/..
 
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4

Molecular, Biochemical, and Clinical Characterization of Th..:

Abdul Wahab, Siti Aishah ; Yakob, Yusnita ; Mohd Khalid, Mohd Khairul Nizam...
Genetics Research.  2022 (2022)  - p. 1-7 , 2022
Link: https://doi.org/10.1155/..
 
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5

Long-term clinical outcomes of patients treated with elosul..:

Mitchell, John ; Ramaswami, Uma ; Longo, Nicola...
Molecular Genetics and Metabolism.  129 (2020)  2 - p. S112 , 2020
Link: https://doi.org/10.1016/..
 
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6

Long-term treatment with elosulfase alfa has an acceptable ..:

Burton, Barbara ; Guffon, Nathalie ; Ramaswami, Uma...
Molecular Genetics and Metabolism.  129 (2020)  2 - p. S36 , 2020
Link: https://doi.org/10.1016/..
 
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7

Clinical, biochemical and genetic profiles of patients with..:

Leong, Huey Yin ; Abdul Azize, Nor Azimah ; Chew, Hui Bein...
Orphanet Journal of Rare Diseases.  14 (2019)  1 - p. , 2019
Link: https://doi.org/10.1186/..
 
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8

Identification of mutations in Malaysian patients with argi..:

Ali, Ernie Zuraida ; Yakob, Yusnita ; Ngu, Lock Hock
Molecular Genetics and Metabolism Reports.  21 (2019)  - p. 100525 , 2019
Link: https://doi.org/10.1016/..
 
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9

Mutation Study of Malaysian Patients with Ornithine Transca..:

Ali, Ernie Zuraida ; Zakaria, Yuslina ; Mohd Radzi, Mohd Amran..
BioMed Research International.  2018 (2018)  - p. 1-15 , 2018
Link: https://doi.org/10.1155/..
 
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10

Fructose-1,6-bisphosphatase deficiency as a cause of recurr..:

Moey, Lip Hen ; Abdul Azize, Nor Azimah ; Yakob, Yusnita...
Pediatrics & Neonatology.  59 (2018)  4 - p. 397-403 , 2018
Link: https://doi.org/10.1016/..
 
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11

Mutations in mitochondrial complex I assembly factor NDUFAF..:

Baertling, Fabian ; Sánchez-Caballero, Laura ; Timal, Sharita...
Molecular Genetics and Metabolism.  120 (2017)  3 - p. 243-246 , 2017
Link: https://doi.org/10.1016/..
 
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12

Two Novel Gross Deletions of TSC2 in Malaysian Patients wit..:

Ismail, Nur Farrah Dila ; Nik Abdul Malik, Nik Mohd Ariff ; Mohseni, Jafar...
Japanese Journal of Clinical Oncology.  44 (2014)  5 - p. 506-511 , 2014
Link: https://doi.org/10.1093/..
 
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13

Mutational Analyses on X-Linked Adrenoleukodystrophy Reveal..:

Hung, Kun-Long ; Wang, Jinn-Shyan ; Keng, Wee Teik...
Pediatric Neurology.  49 (2013)  3 - p. 185-190 , 2013
Link: https://doi.org/10.1016/..
 
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14

A catalytic defect in mitochondrial respiratory chain compl..:

Ngu, Lock Hock ; Nijtmans, Leo G. ; Distelmaier, Felix...
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease.  1822 (2012)  2 - p. 168-175 , 2012
Link: https://doi.org/10.1016/..
 
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15

Neonatal intrahepatic cholestasis associated with citrin de..:

Chew, Hui Bein ; Ngu, Lock Hock ; Zabedah, Md Yunus...
Journal of Inherited Metabolic Disease.  33 (2010)  S3 - p. 489-495 , 2010
Link: https://doi.org/10.1007/..
 
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