Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerations

Yahia, A (author)

Karolinska Institutet

Hamed, AAA (author)

Mohamed, IN (author)

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Elseed, MA (author)

Salih, MA (author)

El-Sadig, S (author)

Siddig, HE (author)

Nasreldien, AEM (author)

Abdullah, MA (author)

Elzubair, M (author)

Omer, FY (author)

Bakhiet, AM (author)

Abubaker, R (author)

Abozar, F (author)

Adil, R (author)

Emad, S (author)

Musallam, MA (author)

Eltazi, IZM (author)

Omer, Z (author)

Malik, H (author)

Mohamed, MOE (author)

Elhassan, AA (author)

Mohamed, EOE (author)

Ahmed, AKMA (author)

Ahmed, EAA (author)

Eltaraifee, E (author)

Hussein, BK (author)

Abd Allah, ASI (author)

Salah, L (author)

Nimir, M (author)

Elseed, OMT (author)

Elhassan, TEA (author)

Elbashier, A (author)

Alfadul, ESA (author)

Fadul, M (author)

Ali, KF (author)

Taha, SOMA (author)

Bushara, EE (author)

Amin, M (author)

Koko, M (author)

Ibrahim, ME (author)

Ahmed, AE (author)

Elsayed, LEO (author)

Stevanin, G (author)

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 (creator_code:org_t)

2023

2023

English.

In: European journal of human genetics : EJHG. - 1476-5438. ; 31:6

Related links:

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https://doi.org/10.1...

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• Journal article (peer-reviewed)