STAMBP gene mutation causing microcephaly-capillary malformation syndrome: a recognizable developmental and epileptic encephalopathy
Vaishakh Anand
Department of Pediatric Neurology, Amrita Institute of Medical Sciences, Kochi, Kerala, India
Child Neurology Division, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India
Search for more papers by this authorBhawana Aggarwa
Division of Medical Genetics, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India
Search for more papers by this authorCorresponding Author
Prashant Jauhari
Child Neurology Division, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India
Correspondence: Prashant Jauhari All India Institute of Medical Sciences Ringgold standard institution – Pediatrics, AIIMS, New Delhi, New Delhi 110029, India <[email protected]>Search for more papers by this authorManoj Kumar
Department of Biophysics, All India Institute of Medical Sciences, New Delhi, India
Search for more papers by this authorNeerja Gupta
Division of Medical Genetics, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India
Search for more papers by this authorAtin Kumar
Department of Radiodiagnosis, All India Institute of Medical Sciences, New Delhi, India
Search for more papers by this authorSheffali Gulati
Child Neurology Division, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India
Search for more papers by this authorMadhulika Kabra
Division of Medical Genetics, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India
Search for more papers by this authorVaishakh Anand
Department of Pediatric Neurology, Amrita Institute of Medical Sciences, Kochi, Kerala, India
Child Neurology Division, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India
Search for more papers by this authorBhawana Aggarwa
Division of Medical Genetics, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India
Search for more papers by this authorCorresponding Author
Prashant Jauhari
Child Neurology Division, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India
Correspondence: Prashant Jauhari All India Institute of Medical Sciences Ringgold standard institution – Pediatrics, AIIMS, New Delhi, New Delhi 110029, India <[email protected]>Search for more papers by this authorManoj Kumar
Department of Biophysics, All India Institute of Medical Sciences, New Delhi, India
Search for more papers by this authorNeerja Gupta
Division of Medical Genetics, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India
Search for more papers by this authorAtin Kumar
Department of Radiodiagnosis, All India Institute of Medical Sciences, New Delhi, India
Search for more papers by this authorSheffali Gulati
Child Neurology Division, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India
Search for more papers by this authorMadhulika Kabra
Division of Medical Genetics, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India
Search for more papers by this author
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References
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