Natural history and genetic study of LAMA2-related muscular dystrophy in a large Chinese cohort.

Tan D, Ge L, Fan Y, Chang X, Wang S, Wei C, Ding J, Liu A, Wang S, Li X, Gao K, Yang H, Que C, Huang Z, Li C, Zhu Y, Mao B, Jin B, Hua Y, Zhang X, Zhang B, Zhu W, Zhang C, Wang Y, Yuan Y, Jiang Y, Rutkowski A, Bönnemann CG, Wu X, Xiong H

Open source

DOI: 10.1186/s13023-021-01950-x
Published: 2021 Jul 19
Container: Orphanet journal of rare diseases
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1186/s13023-021-01950-x,
  title = {Natural history and genetic study of LAMA2-related muscular dystrophy in a large Chinese cohort.},
  author = {Tan D and Ge L and Fan Y and Chang X and Wang S and Wei C and Ding J and Liu A and Wang S and Li X and Gao K and Yang H and Que C and Huang Z and Li C and Zhu Y and Mao B and Jin B and Hua Y and Zhang X and Zhang B and Zhu W and Zhang C and Wang Y and Yuan Y and Jiang Y and Rutkowski A and Bönnemann CG and Wu X and Xiong H},
  year = {2021},
  journal = {Orphanet journal of rare diseases},
  doi = {10.1186/s13023-021-01950-x},
  url = {https://doi.org/10.1186/s13023-021-01950-x}
}

RIS

TY  - JOUR
TI  - Natural history and genetic study of LAMA2-related muscular dystrophy in a large Chinese cohort.
AU  - Tan D
AU  - Ge L
AU  - Fan Y
AU  - Chang X
AU  - Wang S
AU  - Wei C
AU  - Ding J
AU  - Liu A
AU  - Wang S
AU  - Li X
AU  - Gao K
AU  - Yang H
AU  - Que C
AU  - Huang Z
AU  - Li C
AU  - Zhu Y
AU  - Mao B
AU  - Jin B
AU  - Hua Y
AU  - Zhang X
AU  - Zhang B
AU  - Zhu W
AU  - Zhang C
AU  - Wang Y
AU  - Yuan Y
AU  - Jiang Y
AU  - Rutkowski A
AU  - Bönnemann CG
AU  - Wu X
AU  - Xiong H
PY  - 2021
JO  - Orphanet journal of rare diseases
DO  - 10.1186/s13023-021-01950-x
UR  - https://doi.org/10.1186/s13023-021-01950-x
ER  -

APA

D, T., L, G., Y, F., X, C., S, W., C, W., J, D., A, L., S, W., X, L., K, G., H, Y., C, Q., Z, H., C, L., Y, Z., B, M., B, J., Y, H., X, Z., B, Z., W, Z., C, Z., Y, W., Y, Y., Y, J., A, R., CG, B., X, W., & H, X. (2021). Natural history and genetic study of LAMA2-related muscular dystrophy in a large Chinese cohort.. Orphanet journal of rare diseases. https://doi.org/10.1186/s13023-021-01950-x

Source records

pubmed · retrieved 2026-09-26T01:47:12.009Z