Found: 4
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A novel mutation in KIF5A in a Malian family with spastic paraplegia and sensory loss.
- Published in:
- Annals of Clinical & Translational Neurology, 2017, v. 4, n. 4, p. 272, doi. 10.1002/acn3.402
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- Publication type:
- Article
A novel de novo variant in the RUNX2 gene causes cleidocranial dysplasia in a Malian girl.
- Published in:
- 2024
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- Publication type:
- Case Study
Friedreich ataxia in a family from Mali, West Africa/Friedreich ataxia in a Malian family.
- Published in:
- Clinical Case Reports, 2021, v. 9, n. 5, p. 1, doi. 10.1002/ccr3.4065
- By:
- Publication type:
- Article
Novel variant in CADM3 causes Charcot-Marie-Tooth disease.
- Published in:
- Brain Communications, 2023, v. 5, n. 5, p. 1, doi. 10.1093/braincomms/fcad227
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- Publication type:
- Article