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A Novel Homozygous Missense Variant of PIGT Related to Multiple Congenital Anomalies-Hypotonia Seizures Syndrome 3 with Elevated of Serum ALP Level in a Thai Newborn Patient.

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Title:	A Novel Homozygous Missense Variant of PIGT Related to Multiple Congenital Anomalies-Hypotonia Seizures Syndrome 3 with Elevated of Serum ALP Level in a Thai Newborn Patient.
Authors:	Klangjorhor, Jeerawan^1,2,3 (AUTHOR), Wiwattanadittakul, Natrujee^2,4 (AUTHOR), Jaimalai, Thanapak^1,3 (AUTHOR), Thongkumkoon, Patcharawadee^1,4 (AUTHOR), Noisagul, Pitiporn¹ (AUTHOR), Khiaomai, Ratchadaporn^1,2 (AUTHOR), Sirikaew, Nutnicha^1,3 (AUTHOR), Moonsan, Nonthanan⁴ (AUTHOR), Pasena, Arnat¹ (AUTHOR), Suksakit, Pathacha¹ (AUTHOR), Teeyakasem, Pimpisa³ (AUTHOR), Chaiyawat, Parunya^1,3 (AUTHOR), Tengsujaritkul, Maliwan⁴ (AUTHOR)
Source:	International Journal of Molecular Sciences. Mar2025, Vol. 26 Issue 6, p2790. 16p.
Database:	Academic Search Ultimate
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