Homo sapiens cDNA, FLJ94307

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HPDL mutations identified by exome sequencing are associated with infant neurodevelopmental disorders. [Mol Genet Genomic Med. 2022]
HPDL mutations identified by exome sequencing are associated with infant neurodevelopmental disorders.
Wang Y, Zheng X, Feng C, Fan X, Liu L, Guo P, Lei Z, Mei S. Mol Genet Genomic Med. 2022 Oct; 10(10):e2025. Epub 2022 Aug 19.
Novel bi-allelic HPDL variants cause hereditary spastic paraplegia in a Chinese patient. [Clin Genet. 2021]
Novel bi-allelic HPDL variants cause hereditary spastic paraplegia in a Chinese patient.
Yu H, Wei Q, Luo WJ, Wu ZY. Clin Genet. 2021 Dec; 100(6):777-778. Epub 2021 Sep 13.
Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia. [Brain. 2021]
Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia.
Wiessner M, Maroofian R, Ni MY, Pedroni A, Müller JS, Stucka R, Beetz C, Efthymiou S, Santorelli FM, Alfares AA, et al. Brain. 2021 Jun 22; 144(5):1422-1434.

Homo sapiens cDNA, FLJ94307
Homo sapiens cDNA, FLJ94307
gi|164695497|dbj|AK313714.1|

Nucleotide

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Nucleotide