A Sibling Pair with Autosomal Recessive Charcot-Marie-Tooth Disease Due to Novel Ganglioside-induced Differentiation-associated Protein 1 Mutation.

Shah PA, Shah AM

Open source

DOI
10.4103/aian.aian_251_17
Published
2017 Oct-Dec
Container
Annals of Indian Academy of Neurology
Publisher
Not recorded
Open access
yes

Credibility signals

limited evidence Score 45/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.

Show all credibility signals

Cite this work

BibTeX

@article{allodium:10.4103/aian.aian_251_17,
  title = {A Sibling Pair with Autosomal Recessive Charcot-Marie-Tooth Disease Due to Novel Ganglioside-induced Differentiation-associated Protein 1 Mutation.},
  author = {Shah PA and Shah AM},
  year = {2017},
  journal = {Annals of Indian Academy of Neurology},
  doi = {10.4103/aian.aian_251_17},
  url = {https://doi.org/10.4103/aian.aian_251_17}
}

RIS

TY  - JOUR
TI  - A Sibling Pair with Autosomal Recessive Charcot-Marie-Tooth Disease Due to Novel Ganglioside-induced Differentiation-associated Protein 1 Mutation.
AU  - Shah PA
AU  - Shah AM
PY  - 2017
JO  - Annals of Indian Academy of Neurology
DO  - 10.4103/aian.aian_251_17
UR  - https://doi.org/10.4103/aian.aian_251_17
ER  - 

APA

PA, S., & AM, S. (2017). A Sibling Pair with Autosomal Recessive Charcot-Marie-Tooth Disease Due to Novel Ganglioside-induced Differentiation-associated Protein 1 Mutation.. Annals of Indian Academy of Neurology. https://doi.org/10.4103/aian.aian_251_17

Source records