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A novel METTL5 variant disrupting a donor splice site leads to primary microcephaly-related intellectual disability in an Iranian family: clinical features and literature review.
J Genet. 2023;102:45.
J Genet. 2023.
PMID: 37731250
Free article.
Review.
Clinical and molecular assessment of 13 Iranian families with Wolfram syndrome.
Sobhani M, Amin Tabatabaiefar M, Ghafouri-Fard S, Rajab A, Mozafarpour S, Nasrniya S, Kajbafzadeh AM, Noori-Daloii MR.
Sobhani M, et al. Among authors: amin tabatabaiefar m.
Endocrine. 2019 Nov;66(2):185-191. doi: 10.1007/s12020-019-02004-w. Epub 2019 Jul 16.
Endocrine. 2019.
PMID: 31313226
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