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A Rare Case of Neonatal Hypomagnesemia with Secondary Hypocalcemia Caused by a Novel Homozygous TRPM6 Gene Variant.

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Title: A Rare Case of Neonatal Hypomagnesemia with Secondary Hypocalcemia Caused by a Novel Homozygous TRPM6 Gene Variant.
Authors: Uddin MS; Department of Pediatrics, Ministry of National Guard Health Affairs, Dammam, Saudi Arabia., Alradhi AY; Department of Pediatrics, Ministry of National Guard Health Affairs, Dammam, Saudi Arabia., Alqathani FMN; Department of Pediatrics, Ministry of National Guard Health Affairs, Dammam, Saudi Arabia., Alessa OS; Department of Pediatrics, Ministry of National Guard Health Affairs, Dammam, Saudi Arabia., Alshammari ANM; Department of Pediatrics, Ministry of National Guard Health Affairs, Dammam, Saudi Arabia., Tripathy R; Department of Human Genetics, Bioscientia Institute for Medical Diagnostics GmbH, Ingelheim, Germany., Alomari MA; Department of Pediatrics, Ministry of National Guard Health Affairs, Dammam, Saudi Arabia.
Source: The American journal of case reports [Am J Case Rep] 2024 Mar 26; Vol. 25, pp. e942498. Date of Electronic Publication: 2024 Mar 26.
Publication Type: Case Reports; Journal Article
Journal Info: Publisher: International Scientific Information, Inc Country of Publication: United States NLM ID: 101489566 Publication Model: Electronic Cited Medium: Internet ISSN: 1941-5923 (Electronic) Linking ISSN: 19415923 NLM ISO Abbreviation: Am J Case Rep Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: A Rare Case of Neonatal Hypomagnesemia with Secondary Hypocalcemia Caused by a Novel Homozygous TRPM6 Gene Variant.
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  Data: <searchLink fieldCode="AU" term="%22Uddin+MS%22">Uddin MS</searchLink>; Department of Pediatrics, Ministry of National Guard Health Affairs, Dammam, Saudi Arabia.<br /><searchLink fieldCode="AU" term="%22Alradhi+AY%22">Alradhi AY</searchLink>; Department of Pediatrics, Ministry of National Guard Health Affairs, Dammam, Saudi Arabia.<br /><searchLink fieldCode="AU" term="%22Alqathani+FMN%22">Alqathani FMN</searchLink>; Department of Pediatrics, Ministry of National Guard Health Affairs, Dammam, Saudi Arabia.<br /><searchLink fieldCode="AU" term="%22Alessa+OS%22">Alessa OS</searchLink>; Department of Pediatrics, Ministry of National Guard Health Affairs, Dammam, Saudi Arabia.<br /><searchLink fieldCode="AU" term="%22Alshammari+ANM%22">Alshammari ANM</searchLink>; Department of Pediatrics, Ministry of National Guard Health Affairs, Dammam, Saudi Arabia.<br /><searchLink fieldCode="AU" term="%22Tripathy+R%22">Tripathy R</searchLink>; Department of Human Genetics, Bioscientia Institute for Medical Diagnostics GmbH, Ingelheim, Germany.<br /><searchLink fieldCode="AU" term="%22Alomari+MA%22">Alomari MA</searchLink>; Department of Pediatrics, Ministry of National Guard Health Affairs, Dammam, Saudi Arabia.
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  Data: <searchLink fieldCode="JN" term="%22101489566%22">The American journal of case reports</searchLink> [Am J Case Rep] 2024 Mar 26; Vol. 25, pp. e942498. <i>Date of Electronic Publication: </i>2024 Mar 26.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22International+Scientific+Information%2C+Inc%22">International Scientific Information, Inc </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101489566 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1941-5923 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2219415923%22">19415923 </searchLink><i>NLM ISO Abbreviation: </i>Am J Case Rep <i>Subsets: </i>MEDLINE
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        Value: 10.12659/AJCR.942498
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      – Code: eng
        Text: English
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      – TitleFull: A Rare Case of Neonatal Hypomagnesemia with Secondary Hypocalcemia Caused by a Novel Homozygous TRPM6 Gene Variant.
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              Text: 2024 Mar 26
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