<mets:mets OBJID="eprint_5089" LABEL="Eprints Item" xsi:schemaLocation="http://www.loc.gov/METS/ http://www.loc.gov/standards/mets/mets.xsd http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-3.xsd" xmlns:mets="http://www.loc.gov/METS/" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"><mets:metsHdr CREATEDATE="2026-07-05T17:25:49Z"><mets:agent ROLE="CUSTODIAN" TYPE="ORGANIZATION"><mets:name>Repositori BKPK</mets:name></mets:agent></mets:metsHdr><mets:dmdSec ID="DMD_eprint_5089_mods"><mets:mdWrap MDTYPE="MODS"><mets:xmlData><mods:titleInfo><mods:title>Korelasi Genotip-Fenotip Pasien Talasemia Beta&#13;
di Kota Samarinda Kalimantan Timur Tahun 2019&#13;
GENOTYPE-PHENOTYPE CORRELATION OF BETA THALASSEMIA PATIENTS&#13;
IN THE CITY OF SAMARINDA, EAST KALIMANTAN 2019</mods:title></mods:titleInfo><mods:name type="personal"><mods:namePart type="given">Zaenal</mods:namePart><mods:namePart type="family">Adi Susanto</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">Wahyu</mods:namePart><mods:namePart type="family">Siswandari</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">Lantip</mods:namePart><mods:namePart type="family">Rujito</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:abstract>Talasemia merupakan salah satu kelainan darah genetik yang bersifat autosomal resesif dan cukup banyak&#13;
ditemui di seluruh dunia. Studi ini bertujuan untuk mengetahui hubungan jenis mutasi gen hemoglobin&#13;
beta (HBB) dengan derajat klinis dan pemeriksaan darah pada 31 pasien talasemia-beta di Kota Samarinda&#13;
Provinsi Kalimantan Timur pada bulan Mei tahun 2019. Sampel darah pasien diambil untuk memperoleh&#13;
DNA kemudian dilakukan amplifikasi dengan Polymerase Chain Reaction dan dilakukan teknik direct&#13;
sekuensing untuk menganalisis mutasi gen hemoglobin-beta. Etnik Jawa merupakan yang dominan dalam&#13;
penelitian ini (64,5%) dan derajat klinis paling umum adalah kategori sedang (77,4%). Rerata nilai MCV&#13;
dan MCH masing-masing adalah 72±5,5 fL dan 24±3,3 pg. Analisa DNA didapatkan 8 jenis alel mutan&#13;
yaitu Cd26/HbE (GAG&gt;AAG) 48,4% selanjutnya IVS-1-5 (G&gt;C) 14,5%, IVS-1-2 (T&gt;C) 12,9%, Cd35&#13;
(-C) 8,1%, IVS-1-1 (G&gt;T) 6,5%, Cd30 (AGG&gt;ACG) 3,2%, Cd60 (GTG&gt;GAG) dan Cd2 (CAT&gt;CAC)&#13;
masing-masing 1,6%. Studi ini menemukan mutasi yang belum dilaporkan pada penelitian sebelumnya di&#13;
Indonesia yaitu Cd60 (GTG&gt;GAG) dan Cd2 (CAT&gt;CAC). Uji statistik spearman rank menunjukkan tidak&#13;
terdapat hubungan bermakna antara ke dua variabel yang diteliti.</mods:abstract><mods:classification authority="lcc">WH 120-540 Hematologic Diseases. Immunologic Factors. Blood Banks</mods:classification><mods:originInfo><mods:dateIssued encoding="iso8601">2020-06</mods:dateIssued></mods:originInfo><mods:originInfo><mods:publisher>Sekretariat Badan Penelitian dan Pengembangan Kesehatan</mods:publisher></mods:originInfo><mods:genre>Article</mods:genre></mets:xmlData></mets:mdWrap></mets:dmdSec><mets:amdSec ID="TMD_eprint_5089"><mets:rightsMD ID="rights_eprint_5089_mods"><mets:mdWrap MDTYPE="MODS"><mets:xmlData><mods:useAndReproduction>
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