Suchergebnisse - "Xu, Chaolong"

PubPharm (4)

1

Establishment of an iPSC line (BCHNDi001-A) from a patient with nicotinamide nucleotide repair system deficiency caused by biallelic NAXD mutations

enthalten in: Stem cell research | 2024

von Xu, C. | Zhou, L. | Jiang, H. | +4

2

Phenotypic spectrum of iron-sulfur cluster assembly gene IBA57 mutations: c.286T>C identified as a hotspot mutation in Chinese patients with a stable natural history

enthalten in: ResearchSquare.com | 2024

von Jiang, H. | Xu, C. | Duan, R. | +11

3

Generation of an induced pluripotent stem cell line (BCHNCi003-A) from a patient with mitochondrial pyruvate carrier deficiency caused by biallelic MPC1 mutations

enthalten in: Stem cell research | 2023

von Jiang, H. | Xu, C. | Li, W. | +2

4

Thiamine pyrophosphokinase deficiency : report of two Chinese cases and a literature review

enthalten in: Frontiers in pediatrics | 2023

von Zhao, D. | Liu, M. | Jiang, H. | +7

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