Identification of a novel CNTNAP1 mutation causing arthrogryposis multiplex congenita with cerebral and cerebellar atrophy - Concepedia

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Identification of a novel CNTNAP1 mutation causing arthrogryposis multiplex congenita with cerebral and cerebellar atrophy

DOI Full Paper Access

27

Citations

13

References

2017

Year

Shenela Lakhani, Ryan N. Doan, Mariam Al‐Mureikhi, Jennifer N. Partlow, Muna Al Saffar, Mahmoud F. Elsaid, Nada Alaaraj, A. James Barkovich, Christopher A. Walsh, Tawfeg Ben‐Omran

European Journal of Medical Genetics

Neurodegenerative DiseasesCerebellar AtrophyMendelian DisorderGenetic DisorderGeneticsPathologyDegenerative DiseaseNeurologyNovel Cntnap1 MutationDisease Gene IdentificationNeuropathologyMedicineArthrogryposis Multiplex CongenitaNeurogenetics

References

	Year	Citations

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