la-related protein 7 isoform 4 [Homo sapiens]

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Alazami syndrome: Report of three Indian patients with phenotypic spectrum from adolescence to adulthood. [Am J Med Genet A. 2021]
Alazami syndrome: Report of three Indian patients with phenotypic spectrum from adolescence to adulthood.
Das S, Godbole K, Abraham SSC, Ganesan P, Kamdar P, Danda S. Am J Med Genet A. 2021 May; 185(5):1606-1609. Epub 2021 Feb 11.
Novel Mutation in LARP7 in Two Iranian Consanguineous Families with Syndromic Intellectual Disability and Facial Dysmorphism. [Arch Iran Med. 2020]
Novel Mutation in LARP7 in Two Iranian Consanguineous Families with Syndromic Intellectual Disability and Facial Dysmorphism.
Kazemi G, Peymani F, Mohseni M, Zare Ashrafi F, Arzhangi S, Ardalani F, Aghakhani Moghaddam F, Kahrizi K, Najmabadi H. Arch Iran Med. 2020 Dec 1; 23(12):842-847. Epub 2020 Dec 1.
Alazami syndrome: Phenotypic expansion and clinical resemblance to Smith-Lemli-Opitz syndrome. [Am J Med Genet A. 2020]
Alazami syndrome: Phenotypic expansion and clinical resemblance to Smith-Lemli-Opitz syndrome.
Gana S, Plumari M, Rossi E, Saracino A, Iorio M, Zanaboni MP, Orcesi S, Valente EM. Am J Med Genet A. 2020 Nov; 182(11):2722-2726. Epub 2020 Sep 5.

RefSeq genomic sequence
See the genomic reference sequence for the LARP7 gene (NG_032779.1).
RefSeq mRNA
See reference mRNA sequence for the LARP7 gene (NM_001370976.1).
RefSeq protein isoforms
See 22 reference sequence protein isoforms for the LARP7 gene.

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Protein