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Table1_Case report: Incomplete penetrance of autosomal domi..:

Nurul Huda Musa (14317911) ; Karuppiah Thilakavathy (14317914) ; Nur Afiqah Mohamad (10987995)...
https://figshare.com/articles/dataset/Table1_Case_report_Incomplete_penetrance_of_autosomal_dominant_myotonia_congenita_caused_by_a_rare_CLCN1_variant_c_1667T_A_p_I556N_in_a_Malaysian_family_XLSX/21804582. , 2023

Link: https://doi.org/10.3389/fgene.2022.972007.s001

RT Journal
T1 <Title>Table1_Case report: Incomplete penetrance of autosomal dominant myotonia congenita caused by a rare CLCN1 variant c.1667T>A (p.I556N) in a Malaysian family.XLSX</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftunivfreestate:oai:figshare.com:article_21804582&Exemplar=1&LAN=DE
				
A1 Nurul Huda Musa (14317911)
A1 Karuppiah Thilakavathy (14317914)
A1 Nur Afiqah Mohamad (10987995)
A1 Marina L. Kennerson (3149982)
A1 Liyana Najwa Inche Mat (9462848)
A1 Wei Chao Loh (9462839)
A1 Anna Misyail Abdul Rashid (10987998)
A1 Janudin Baharin (9462845)
A1 Azliza Ibrahim (9930845)
A1 Wan Aliaa Wan Sulaiman (9462851)
A1 Fan Kee Hoo (9462860)
A1 Hamidon Basri (6122072)
A1 Abdul Hanif Khan Yusof Khan (9462833)
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 https://figshare.com/articles/dataset/Table1_Case_report_Incomplete_penetrance_of_autosomal_dominant_myotonia_congenita_caused_by_a_rare_CLCN1_variant_c_1667T_A_p_I556N_in_a_Malaysian_family_XLSX/21804582
LK http://dx.doi.org/https://doi.org/10.3389/fgene.2022.972007.s001
DO https://doi.org/10.3389/fgene.2022.972007.s001
SF ELIB - SuUB Bremen

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