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Table3_Case report: Incomplete penetrance of autosomal domi..:
Nurul Huda Musa
;
Karuppiah Thilakavathy
;
Nur Afiqah Mohamad
...
doi:10.3389/fgene.2022.972007.s003. , 2023
Link:
https://doi.org/10.3389/fgene.2022.972007.s003
RT Journal T1
Table3_Case report: Incomplete penetrance of autosomal dominant myotonia congenita caused by a rare CLCN1 variant c.1667T>A (p.I556N) in a Malaysian family.DOCX
UL https://suche.suub.uni-bremen.de/peid=base-ftfrontimediafig:oai:figshare.com:article_21804588&Exemplar=1&LAN=DE A1 Nurul Huda Musa A1 Karuppiah Thilakavathy A1 Nur Afiqah Mohamad A1 Marina L. Kennerson A1 Liyana Najwa Inche Mat A1 Wei Chao Loh A1 Anna Misyail Abdul Rashid A1 Janudin Baharin A1 Azliza Ibrahim A1 Wan Aliaa Wan Sulaiman A1 Fan Kee Hoo A1 Hamidon Basri A1 Abdul Hanif Khan Yusof Khan YR 2023 K1 Genetics K1 Genetic Engineering K1 Biomarkers K1 Developmental Genetics (incl. Sex Determination) K1 Epigenetics (incl. Genome Methylation and Epigenomics) K1 Gene Expression (incl. Microarray and other genome-wide approaches) K1 Genome Structure and Regulation K1 Genomics K1 Genetically Modified Animals K1 Livestock Cloning K1 Gene and Molecular Therapy K1 myotonia congenita K1 CLCN1 K1 Thomsen disease K1 autosomal dominant K1 chloride channel K1 case report JF doi:10.3389/fgene.2022.972007.s003 LK http://dx.doi.org/https://doi.org/10.3389/fgene.2022.972007.s003 DO https://doi.org/10.3389/fgene.2022.972007.s003 SF ELIB - SuUB Bremen
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