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23. MYH7B variants cause hypertrophic cardiomyopathy by activating the CaMK-signaling pathway. Chen P; Li Z; Nie J; Wang H; Yu B; Wen Z; Sun Y; Shi X; Jin L; Wang DW Sci China Life Sci; 2020 Sep; 63(9):1347-1362. PubMed ID: 32207065 [TBL] [Abstract][Full Text] [Related]
24. A novel heterozygous missense MYH7 mutation potentially causes an autosomal dominant form of myosin storage myopathy with dilated cardiomyopathy. Naderi N; Mohsen-Pour N; Nilipour Y; Pourirahim M; Maleki M; Kalayinia S BMC Cardiovasc Disord; 2023 Oct; 23(1):487. PubMed ID: 37794383 [TBL] [Abstract][Full Text] [Related]
25. Identification of novel mutations including a double mutation in patients with inherited cardiomyopathy by a targeted sequencing approach using the Ion Torrent PGM system. Zhao Y; Cao H; Song Y; Feng Y; Ding X; Pang M; Zhang Y; Zhang H; Ding J; Xia X Int J Mol Med; 2016 Jun; 37(6):1511-20. PubMed ID: 27082122 [TBL] [Abstract][Full Text] [Related]
26. Novel Desmin Mutation p.Glu401Asp Impairs Filament Formation, Disrupts Cell Membrane Integrity, and Causes Severe Arrhythmogenic Left Ventricular Cardiomyopathy/Dysplasia. Bermúdez-Jiménez FJ; Carriel V; Brodehl A; Alaminos M; Campos A; Schirmer I; Milting H; Abril BÁ; Álvarez M; López-Fernández S; García-Giustiniani D; Monserrat L; Tercedor L; Jiménez-Jáimez J Circulation; 2018 Apr; 137(15):1595-1610. PubMed ID: 29212896 [TBL] [Abstract][Full Text] [Related]
27. Biallelic mutation in MYH7 and MYBPC3 leads to severe cardiomyopathy with left ventricular noncompaction phenotype. Kolokotronis K; Kühnisch J; Klopocki E; Dartsch J; Rost S; Huculak C; Mearini G; Störk S; Carrier L; Klaassen S; Gerull B Hum Mutat; 2019 Aug; 40(8):1101-1114. PubMed ID: 30924982 [TBL] [Abstract][Full Text] [Related]
28. Coexistence of Digenic Mutations in Both Thin (TPM1) and Thick (MYH7) Filaments of Sarcomeric Genes Leads to Severe Hypertrophic Cardiomyopathy in a South Indian FHCM. Selvi Rani D; Nallari P; Dhandapany PS; Rani J; Meraj K; Ganesan M; Narasimhan C; Thangaraj K DNA Cell Biol; 2015 May; 34(5):350-9. PubMed ID: 25607779 [TBL] [Abstract][Full Text] [Related]
29. Wang J; Zhang X; Wang X; Wang C; Wang F; Wang B Circ Cardiovasc Genet; 2017 Dec; 10(6):. PubMed ID: 29237678 [No Abstract] [Full Text] [Related]
30. [Analysis of genotype-phenotype correlation for a novel MYH7-D554Y mutation identified in an ethnic Han Chinese pedigree affected with hypertrophic cardiomyopathy]. Yang Q; Wang B; Wang J; Sun C; Ma Z; Zuo L; Zhang Y; Liu L Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Oct; 35(5):667-671. PubMed ID: 30298491 [TBL] [Abstract][Full Text] [Related]
31. A low prevalence of MYH7/MYBPC3 mutations among familial hypertrophic cardiomyopathy patients in India. Bashyam MD; Purushotham G; Chaudhary AK; Rao KM; Acharya V; Mohammad TA; Nagarajaram HA; Hariram V; Narasimhan C Mol Cell Biochem; 2012 Jan; 360(1-2):373-82. PubMed ID: 21959974 [TBL] [Abstract][Full Text] [Related]
32. Digenic Inheritance of LAMA4 and MYH7 Mutations in Patient with Infantile Dilated Cardiomyopathy. Abdallah AM; Carlus SJ; Al-Mazroea AH; Alluqmani M; Almohammadi Y; Bhuiyan ZA; Al-Harbi KM Medicina (Kaunas); 2019 Jan; 55(1):. PubMed ID: 30650640 [No Abstract] [Full Text] [Related]
33. Sarcomere mutations in cardiogenesis and ventricular noncompaction. McNally E; Dellefave L Trends Cardiovasc Med; 2009 Jan; 19(1):17-21. PubMed ID: 19467449 [TBL] [Abstract][Full Text] [Related]
34. Detection of mutations in symptomatic patients with hypertrophic cardiomyopathy in Taiwan. Chiou KR; Chu CT; Charng MJ J Cardiol; 2015 Mar; 65(3):250-6. PubMed ID: 25086479 [TBL] [Abstract][Full Text] [Related]
35. Molecular analysis of inherited cardiomyopathy using next generation semiconductor sequencing technologies. Lu C; Wu W; Liu F; Yang K; Li J; Liu Y; Wang R; Si N; Gao P; Liu Y; Zhang S; Zhang X J Transl Med; 2018 Aug; 16(1):241. PubMed ID: 30165862 [TBL] [Abstract][Full Text] [Related]
36. Genotype phenotype correlations of cardiac beta-myosin heavy chain mutations in Indian patients with hypertrophic and dilated cardiomyopathy. Rai TS; Ahmad S; Bahl A; Ahuja M; Ahluwalia TS; Singh B; Talwar KK; Khullar M Mol Cell Biochem; 2009 Jan; 321(1-2):189-96. PubMed ID: 18953637 [TBL] [Abstract][Full Text] [Related]
37. MYH7-related disorders in two Bulgarian families: Novel variants in the same region associated with different clinical manifestation and disease penetrance. Atemin S; Todorov T; Maver A; Chamova T; Georgieva B; Tincheva S; Pacheva I; Ivanov I; Taneva A; Zlatareva D; Tournev I; Guergueltcheva V; Gospodinova M; Chochkova L; Peterlin B; Mitev V; Todorova A Neuromuscul Disord; 2021 Jul; 31(7):633-641. PubMed ID: 34053846 [TBL] [Abstract][Full Text] [Related]
38. Cardiomyopathy: a systematic review of disease-causing mutations in myosin heavy chain 7 and their phenotypic manifestations. Walsh R; Rutland C; Thomas R; Loughna S Cardiology; 2010; 115(1):49-60. PubMed ID: 19864899 [TBL] [Abstract][Full Text] [Related]