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Year | Number of Results |
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1993 | 1 |
1998 | 1 |
2014 | 1 |
2023 | 1 |
2024 | 0 |
PubMed for id: 742068551
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Homozygous splice mutation in CWF19L1 in a Turkish family with recessive ataxia syndrome.
Neurology. 2014 Dec 2;83(23):2175-82. doi: 10.1212/WNL.0000000000001053. Epub 2014 Oct 31.
Neurology. 2014.
PMID: 25361784
Free PMC article.
Hereditary Ataxia Overview.
Perlman S.
Perlman S.
1998 Oct 28 [updated 2023 Nov 16]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024.
1998 Oct 28 [updated 2023 Nov 16]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024.
PMID: 20301317
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