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Leeb T, Brenig B (1998). "cDNA cloning and sequencing of the human ryanodine receptor type 3 (RYR3) reveals a novel alternative splice site in the RYR3 gene". FEBS Lett. 423 (3): 367–70.
doi:
10.1016/S0014-5793(98)00124-0.
PMID9515741.
S2CID19974365.
Davis MR, Haan E, Jungbluth H, et al. (2003). "Principal mutation hotspot for central core disease and related myopathies in the C-terminal transmembrane region of the RYR1 gene". Neuromuscul. Disord. 13 (2): 151–7.
doi:
10.1016/S0960-8966(02)00218-3.
PMID12565913.
S2CID30235519.
Masumiya H, Yamamoto H, Hemberger M, et al. (2003). "The mouse sino-atrial node expresses both the type 2 and type 3 Ca(2+) release channels/ryanodine receptors". FEBS Lett. 553 (1–2): 141–4.
doi:
10.1016/S0014-5793(03)00999-2.
PMID14550562.
S2CID20575812.
Martin C, Chapman KE, Seckl JR, Ashley RH (1998). "Partial cloning and differential expression of ryanodine receptor/calcium-release channel genes in human tissues including the hippocampus and cerebellum". Neuroscience. 85 (1): 205–16.
doi:
10.1016/S0306-4522(97)00612-X.
PMID9607712.
S2CID25634042.
Leeb T, Brenig B (1998). "cDNA cloning and sequencing of the human ryanodine receptor type 3 (RYR3) reveals a novel alternative splice site in the RYR3 gene". FEBS Lett. 423 (3): 367–70.
doi:
10.1016/S0014-5793(98)00124-0.
PMID9515741.
S2CID19974365.