A founder RAB27A variant causes Griscelli syndrome type 2 with phenotypic heterogeneity in Qatari families

<p>Griscelli syndrome type 2 (GS2) is a rare autosomal recessive disorder caused by pathogenic variants in the <em>RAB27A</em> gene and characterized by partial albinism, immunodeficiency, and occasional hematological and neurological involvement. We reviewed and analyzed the medic...

وصف كامل

محفوظ في:
التفاصيل البيبلوغرافية
المؤلف الرئيسي: Reem Al‐Sulaiman (14776948) (author)
مؤلفون آخرون: Amna Othman (14152659) (author), Karen El‐Akouri (14776951) (author), Shehab Fareed (14776954) (author), Hajer AlMulla (14776957) (author), Aseel Sukik (14571102) (author), Mariam Al‐Mureikhi (14776960) (author), Noora Shahbeck (14152671) (author), Rehab Ali (14152668) (author), Fatma Al‐Mesaifri (14776963) (author), Sara Musa (14152662) (author), Mariam Al‐Mulla (14776966) (author), Khalid Ibrahim (3853360) (author), Khalid Mohamed (7572353) (author), Maryam Ali Al‐Nesef (14776969) (author), Mohammad Ehlayel (14776972) (author), Tawfeg Ben‐Omran (14776975) (author)
منشور في: 2020
الموضوعات:
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