Rare Compound Heterozygous Frameshift Mutations in ALMS1 Gene Identified Through Exome Sequencing in a Taiwanese Patient With Alström Syndrome

Rare ALMS1 variants https://t.co/9rBX8vYOGS identified through #exome #sequencing in #Taiwanese patient with Alström Syndrome #raredisease https://t.co/JR564LawC7

Rare Compound Heterozygous Frameshift Mutations in ALMS1 Gene Identified Through Exome Sequencing in a Taiwanese Patient With Alström Syndrome. https://t.co/Sbo4ZRDnA3 https://t.co/zBWwsAPQeI

Rare Compound Heterozygous Frameshift Mutations in ALMS1 Gene Identified Through Exome Sequencing in a Taiwanese Patient With Alström Syndrome. https://t.co/B8j6tBheJ6

Rare Compound Heterozygous Frameshift Mutations in ALMS1 Gene Identified Through Exome Sequencing in a Taiwanese Patient With Alström Syndrome: Meng-Che Tsai, Hui-Wen Yu, Tsunglin Liu, Yen-Yin Chou, Yuan-Yow Chiou, Peng-Chieh Chen https://t.co/BjVxXiVkDT