Found: 5
Select item for more details and to access through your institution.
RETINOSCHISIS JUVENILE ET TROU MACULAIRE : à propos d’un cas.
- Published in:
- Mali Médical, 2017, v. 32, n. 4, p. 30
- By:
- Publication type:
- Article
A novel de novo variant in the RUNX2 gene causes cleidocranial dysplasia in a Malian girl.
- Published in:
- 2024
- By:
- 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
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
- By:
- Publication type:
- Article
Hereditary spastic paraplegia in Mali: epidemiological and clinical features.
- Published in:
- Acta Neurologica Belgica, 2023, v. 123, n. 6, p. 2155, doi. 10.1007/s13760-022-02113-w
- By:
- Publication type:
- Article