{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,9,18]],"date-time":"2025-09-18T10:56:41Z","timestamp":1758193001672,"version":"3.44.0"},"reference-count":24,"publisher":"Necmettin Erbakan University Press","issue":"01","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Pediatr Genet"],"published-print":{"date-parts":[[2024,3]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>HOMG1 (hypomagnesemia 1, intestinal) or hypomagnesemia with secondary hypocalcemia is a rare autosomal recessive disorder of magnesium metabolism, characterized by impaired magnesium absorption. This disorder may mimic other conditions presenting with neonatal seizures. Here, we report an infant diagnosed to have hypomagnesemia with secondary hypocalcemia due to novel variants in TRPM6 gene.<\/jats:p>","DOI":"10.1055\/s-0041-1733949","type":"journal-article","created":{"date-parts":[[2021,8,31]],"date-time":"2021-08-31T18:38:29Z","timestamp":1630435109000},"page":"035-042","source":"Crossref","is-referenced-by-count":0,"title":["Hypomagnesemia with Secondary Hypoparathyroidism and Hypocalcemia due to Novel Variants in the Transient Receptor Potential Cation Channel Subfamily M Member 6 (TRPM6) Gene"],"prefix":"10.53391","volume":"13","author":[{"given":"Geetanjali","family":"Jain","sequence":"additional","affiliation":[{"name":"Military Hospital, Nasirabad, India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Gourab","family":"Das","sequence":"additional","affiliation":[{"name":"Army Hospital (Research and Referral), New Delhi, India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Rakhi","family":"Malhotra","sequence":"additional","affiliation":[{"name":"Department of Endocrinology, Army Hospital (Research and Referral), New Delhi, Delhi, India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sateesh","family":"Ramchandran","sequence":"additional","affiliation":[{"name":"Department of Endocrinology, Army Hospital (Research and Referral), New Delhi, Delhi, India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nagaraja M.","family":"Phani","sequence":"additional","affiliation":[{"name":"Department of Molecular Genetics, Life cell Diagnostics Pvt. 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Ltd., Chennai, Tamil Nadu, India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Aradhana","family":"Dwivedi","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Division of Clinical Genetics, Army Hospital (Research and Referral), New Delhi, India"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"31409","published-online":{"date-parts":[[2021,8,31]]},"reference":[{"issue":"02","key":"ref1","first-page":"385","article-title":"Primary hypomagnesemia with secondary hypocalcemia in an infant","volume":"41","author":"L Paunier","year":"1968","journal-title":"Pediatrics"},{"issue":"10","key":"ref2","doi-asserted-by":"crossref","first-page":"3061","DOI":"10.1681\/ASN.2004110989","article-title":"Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemia","volume":"16","author":"K P Schlingmann","year":"2005","journal-title":"J Am Soc 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